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Sample records for polyethylene pe films

  1. The characterisation of two different degradable polyethylene (PE) sacks

    SciTech Connect

    Davis, G. . E-mail: gudavis@cytanet.com.cy

    2006-12-15

    The compostability of two different polyethylene (PE) products on the UK market under open-windrow composting conditions is explored within this paper. Chemical analysis of the PE bags has established their constituents in order to examine how the PE bags have an increased degradability depending on additives. Weight loss of the two different PE products within open-windrow composting conditions was recorded in order to establish the percentage weight loss as an indication of the degradability of the two products and their relative suitability for open-windrow composting. Scanning electron microscopy (SEM) of the PE products over the composting duration established the degradation processes for the PE products within the compost. These analyses concluded that one of the PE product mixes was more degradable than the other. However, neither product completed degraded within the timeframe of 12-14 weeks generally accepted for open-windrow composting in the UK.

  2. The adhesion of oxygen-plasma treated poly(ethylene) and poly(ethylene terephthlate) films

    SciTech Connect

    Holton, S.L.; Kinloch, A.J.; Watts, J.F.

    1996-12-31

    The effects of low-pressure oxygen-plasma treatment on the surfaces of poly(ethylene) (PE) and poly(ethylene terephthlate) (PET) films and its influence on the adhesion of PE/PET laminates were assessed. The 90{degree} peel test was used to estimate the adhesive fracture energy, G{sub c} for the laminates. XPS, SEM and AFM were used to analyse the treated films and fracture surfaces. Significant improvements in bond strength occurred within very short treatment times (5s at 50W) with the maximum adhesion occurring after 300s. For longer treatment times the bond strengths decrease slightly. G{sub c} values were found to be low when PET was the peel arm. When PE was the peel arm, the G{sub c} values were substantially larger using the current analysis.

  3. Development and anti-listerial activity of PE-based biological preservative films incorporating plantaricin BM-1.

    PubMed

    Zhang, Min; Gao, Xiuzhi; Zhang, Hongxing; Liu, Hui; Jin, Junhua; Yang, Wenge; Xie, Yuanhong

    2016-12-18

    In recent years, bacteriocin as a natural antimicrobial compound, provides enormous promise to be used in food safety preservation. In this work, the polyethylene(PE)-based biological preservative films incorporating plantaricin BM-1, a typical IIa bacteriocin produced by Lactobacillus plantarum BM-1, were developed and characterized. The results showed that polyethylene (PE), low-density polyethylene (LDPE) and high-density polyethylene (HDPE) films soaked in plantaricin BM-1 solution had obvious antimicrobial activities aganist Listeria monocytogenes And the volume of plantaricin BM-1 solution absorbed by PE, LDPE and HDPE films continued to increase and reached the maximum during exposure for up to 10, 6 and 16 hours, respectively. And the maximum absorption volumes of plantaricin BM-1 solution had no significant difference (p>0.05) between the PE, LDPE and HDPE films. When soaking in water, the release amount of plantaricin BM-1 from active PE, LDPE and HDPE films reached the maximum potency at 16, 12 and 20 hours respectively. And the maximum release amount of plantaricin BM-1 from PE and LDPE active films were dramatically more than the HDPE active film (p<0.05). Moreover, the inhibitory effect of active films incorporating plantaricin BM-1 maintained stability for at least 120 days against L. monocytogenes stored at 25°C, which suggest a potential application of the biological preservative films on the control of foodborne pathogens L. monocytogenes.

  4. Surface modification of a polyethylene film for anticoagulant and anti-microbial catheter

    PubMed Central

    Zheng, Yingying; Miao, Jianjun; Zhang, Fuming; Cai, Chao; Koh, Amanda; Simmons, Trevor J.; Mousa, Shaker A.; Linhardt, Robert J.

    2016-01-01

    A functional anticoagulant and anti-bacterial coating for polyethylene (PE) films is described. The stepwise preparation of this nanocomposite surface coating involves O2 plasma etching of PE film, carbodiimide coupling of cysteamine to the etched PE film, binding of Ag to sulfhydryl groups of cysteamine, and assembly of heparin capped AgNPs on the PE film. The nanocomposite film and its components were characterized by 1H-nuclear magnetic resonance spectroscopy, attenuated total reflectance-Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and field emission-scanning electron microscopy. The resulting PE films demonstrate anticoagulant activity using a hemoglobin whole blood clotting assay, and anti-bacterial activity against Bacillus cereus 3551 (Gram-positive) and Escherichia coli BL21 (Gram-negative) bacteria. The hydrophilicity of the heparin coated PE was determined by contact angle measurements; and the stability of the nanocomposite film, with respect to Ag leaching, was assessed by atomic absorption spectroscopy. PMID:26900340

  5. Combining polyethylene and polypropylene: Enhanced performance with PE/iPP multiblock polymers.

    PubMed

    Eagan, James M; Xu, Jun; Di Girolamo, Rocco; Thurber, Christopher M; Macosko, Christopher W; LaPointe, Anne M; Bates, Frank S; Coates, Geoffrey W

    2017-02-24

    Polyethylene (PE) and isotactic polypropylene (iPP) constitute nearly two-thirds of the world's plastic. Despite their similar hydrocarbon makeup, the polymers are immiscible with one another. Thus, common grades of PE and iPP do not adhere or blend, creating challenges for recycling these materials. We synthesized PE/iPP multiblock copolymers using an isoselective alkene polymerization initiator. These polymers can weld common grades of commercial PE and iPP together, depending on the molecular weights and architecture of the block copolymers. Interfacial compatibilization of phase-separated PE and iPP with tetrablock copolymers enables morphological control, transforming brittle materials into mechanically tough blends.

  6. Swelling, ion uptake and biodegradation studies of PE film modified through radiation induced graft copolymerization

    NASA Astrophysics Data System (ADS)

    Kaur, Inderjeet; Gupta, Nitika; Kumari, Vandna

    2011-09-01

    An attempt to develop biodegradable polyethylene film grafting of mixture of hydrophilic monomers methacrylic acid (MAAc) and acrylamide (AAm) onto PE film has been carried out by preirradiation method using benzoyl peroxide as the radical initiator. Since ether linkages are susceptible to easy cleavage during degradation process, PE film was irradiated before the grafting reactions by γ-rays to introduce peroxidic linkages (PE-OO-PE) that offer sites for grafting. The effect of irradiation dose, monomer concentration, initiator concentration, temperature, time and amount of water on the grafting percent was determined. Maximum percentage of grafting of binary mixture (MAAc+AAm), (1792%) was obtained at a total concentration of binary monomer mixture=204.6×10 -2 mol/L ([MAAc]=176.5×10 -2 mol/L, [AAm]=28.1×10 -2 mol/L), [BPO]=8.3×10 -2 mol/L at 100 °C in 70 min. The grafted PE film was characterized by the Fourier Transform Infrared Spectroscopy (FTIR), Thermogravimetric Analysis (TGA) and Scanning Electron Microscopic (SEM) methods. Some selective properties of grafted films such as swelling studies, ion uptake and biodegradation studies have been investigated. The grafted films show good swelling in water, ion uptake studies shows promising results for desalination of brackish water and the soil burial test shows that PE film grafted with binary monomer mixture degrades up to 47% within 50 days.

  7. Surface modification by γ-ray-induced grafting of PDMAEMA/PEGMEMA onto PE films

    NASA Astrophysics Data System (ADS)

    Titaux, G. A.; Contreras-García, A.; Bucio, E.

    2009-07-01

    Radiation grafting of poly[2-(dimethylamino) ethyl methacrylate] (PDMAEMA) and poly(ethylene glycol) methyl ether methacrylate (PEGMEMA) onto polyethylene (PE) films was synthesized using gamma radiation from a 60Co source. PE was modified by the PDMAEMA and PEGMEMA by pre-irradiation and one-step method. Grafting as a function of the pre-irradiation dose between 50 and 200 kGy, dose rate of 9 kGy h -1, and monomer concentration 50% of PDMAEMA/PEGMEMA (1/1) in toluene. The characterization of the graft copolymer obtained was carried out by FTIR-ATR, TGA, and DSC. Stimuli-responsive behavior and critical pH point were studied by swelling in water, pH and thermo-responsive films of PE-g-(DMAEMA/PEGMEMA) presented a lower critical solution temperature (LCST) of 55 °C and critical pH point around 8.5.

  8. Surface modification of polyethylene film by acrylamide graft and alcoholysis for improvement of antithrombogenicity

    NASA Astrophysics Data System (ADS)

    Zhao, Guowei; Chen, Yashao; Wang, Xiaoli

    2007-03-01

    To improve antithrombogenicity of polyethylene (PE) films, the films pretreated by Ar plasma were radiated by ultraviolet light to initiate grafting polymerization with acrylamide (AAm) in absence of photo-initiator, then the AAm-grafted PE films (PE-g-AAm) were alcoholized with octadecyl alcohol. Effects of Ar plasma composite parameter ( W/ FM), pretreated time, AAm monomer concentration, and UV irradiation time on grafting rate were investigated systematically. AAm-grafted PE film and alcoholized PE film (PE-g-SAAm) were characterized by contact angle, X-ray photoelectron spectroscopy (XPS), attenuated total reflectance Fourier transfer infrared (ATR-FT-IR) spectroscopy and atomic force microscope (AFM), respectively. The results indicated that the moieties of AAm and stearyl were successively immobilized onto the PE surface. The platelet adhesion experiment showed that antithrombogenicity of the modified PE films was improved in comparison with PE films. The change in antithrombogenicity is attributed to the surface of the modified film in presence of tail-like structure which consists of polyacrylamide as spacer and stearyl as end groups.

  9. Study on the oriented recrystallization of carbon-coated polyethylene oriented ultrathin films.

    PubMed

    Chang, Haibo; Guo, Qipeng; Shen, Deyan; Li, Lin; Qiu, Zhaobin; Wang, Feng; Yan, Shouke

    2010-10-21

    It is confirmed that a layer of vacuum-evaporated carbon on the surface of a preoriented ultrathin polymer film can lead to an oriented recrystallization of the polymer film. This has been attributed to a strong fixing effect of vacuum-evaporated carbon layer on the film surface of the polymer. To study the origin of the strong fixing effect of vacuum-evaporated carbon layer on the polymer films, the melting and recrystallization behaviors of the preoriented ultrathin PE film with a vacuum-evaporated carbon layer were studied by using atomic force microscopy, electron diffraction, Fourier transform infrared spectroscopy, and Raman spectroscopy. We found that there exists some extent of chain orientation of carbon-coated polyethylene (PE) preoriented ultrathin film above its melting temperature. These oriented PE chain sequences act as nucleation sites and induce the oriented recrystallization of preoriented PE film from melt. Raman spectroscopy results suggest that new carbon-carbon bonds between the carbon layer and the oriented PE film are created during the process of vacuum carbon evaporation. As a result, some of the PE chain stems are fixed to the coated carbon substrate via covalent bond. Such a bonding has retarded the relaxation of the PE chains at the spot and, therefore, preserves the original orientation of the PE stems at high temperature, which in turn derives the recrystallization of the PE chains in an oriented structure.

  10. Study on ternary low density polyethylene/linear low density polyethylene/thermoplastic starch blend films.

    PubMed

    Sabetzadeh, Maryam; Bagheri, Rouhollah; Masoomi, Mahmood

    2015-03-30

    In this work, low-density polyethylene/linear low-density polyethylene/thermoplastic starch (LDPE/LLDPE/TPS) films are prepared with the aim of obtaining environmentally friendly materials containing high TPS content with required packaging properties. Blending of LDPE/LLDPE (70/30 wt/wt) with 5-20 wt% of TPS and 3 wt% of PE-grafted maleic anhydride (PE-g-MA) is performed in a twin-screw extruder, followed by the blowing process. Differential scanning calorimetric results indicate starch has more pronounced effect on crystallization of LLDPE than LDPE. Scanning electron micrograph shows a fairly good dispersion of TPS in PE matrices. Fourier transfer infrared spectra confirm compatibility between polymers using PE-g-MA as the compatibilizer. Storage modulus, loss modulus and complex viscosity increase with incorporation of starch. Tensile strength and elongation-at-break decrease from 18 to 10.5 MPa and 340 to 200%, respectively when TPS increases from 5 to 20%. However, the required mechanical properties for packaging applications are attained when 15 wt% starch is added, as specified in ASTM D4635. Finally 12% increase in water uptake is achieved with inclusion of 15 wt% starch.

  11. Oxidized polyethylene films for orienting polar molecules for linear dichroism spectroscopy.

    PubMed

    Razmkhah, Kasra; Chmel, Nikola Paul; Gibson, Matthew I; Rodger, Alison

    2014-03-21

    Stretched polyethylene (PE) films have been used to orient small molecules for decades by depositing solutions on their surface and allowing the solvent to evaporate leaving the analyte absorbed on the polymer film. However, the non-polar hydrophobic nature of PE is an obstacle to aligning polar molecules and biological samples. In this work PE film was treated with oxygen plasma in order to increase surface hydrophilicity. Different treatment conditions were evaluated using contact angle measurement and X-ray photoelectron spectroscopy. Treated PE (PE(OX)) films are shown to be able to align molecules of different polarities including progesterone, 1-pyrenecarboxaldehyde, 4',6-diamidino-2-phenylindole (DAPI) and anthracene. The degree of alignment of each molecule was studied by running series of linear dichroism (LD) experiments and the polarizations of electronic transition moments were determined. For the first time optimal conditions (such as stretching factor and concentration of the sample) for stretched film LD were determined. PE(OX) aligning ability was compared to that of normal PE films. Progesterone showed a slightly better alignment on PE(OX) than PE. 1-Pyrenecarboxaldehyde oriented differently on the two different films which enabled transition moment assignment for this low symmetry molecule. DAPI (which does not align on PE) aligned well on PE(OX) and enabled us to obtain better LD data than had previously been collected with polyvinyl alcohol. Anthracene alignment and formation of dimers and higher order structures were studied in much more detail than previously possible, showing a variety of assemblies on PE and PE(OX) films.

  12. One year monitoring by FTIR of γ-irradiated multilayer film PE/EVOH/PE

    NASA Astrophysics Data System (ADS)

    Gaston, Fanny; Dupuy, Nathalie; Marque, Sylvain R. A.; Barbaroux, Magali; Dorey, Samuel

    2016-08-01

    The multilayer films made of polyethylene/polyethylene-co-vinyl alcohol/polyethylene are γ-irradiated for biopharmaceutical and biotechnological applications. The radiations generate changes in the polymer films. In this study, we focused on the modifications produced on the surface of materials by Fourier transformed infrared (FTIR) spectroscopy combined with chemometric treatments. Principal component analysis (PCA) allows the ordering of the surface modifications according to absorbed doses and the natural ageing. Results show the rising of the acid band and the variation of unsaturated compounds.

  13. Effect of ultraviolet radiation in the photo-oxidation of High Density Polyethylene and Biodegradable Polyethylene films

    NASA Astrophysics Data System (ADS)

    Martínez-Romo, A.; González Mota, R.; Bernal, J. J. Soto; Frausto Reyes, C.; Rosales Candelas, I.

    2015-01-01

    One of the most widely used plastics in the world is the High density polyethylene (HDPE), it is a stable material due to its carbon-carbon bonds, causing their slow degradation; which is why we are looking for alternative ways to accelerate the degradation process of this polymer. An alternative is the addition of oxidized groups in its molecular structure, which results in the development of polymers susceptible to biodegradation (PE-BIO). In this paper, HDPE and PE-BIO films were exposed to UV-B radiation (320-280 nm) at different exposure times, 0-60 days. The effects of UV radiation in samples of HDPE and PE-BIO were characterized using infrared spectroscopy with attenuated total reflectance (ATR). The results show that the exposed materials undergo changes in their molecular structure, due to the infrared bands formed which corresponds to the photo-oxidation of HDPE and PE films when submitted to UV-B radiation.

  14. Preparation of chitosan-coated polyethylene packaging films by DBD plasma treatment.

    PubMed

    Theapsak, Siriporn; Watthanaphanit, Anyarat; Rujiravanit, Ratana

    2012-05-01

    Polyethylene (PE) packaging films were coated with chitosan in order to introduce the antibacterial activity to the films. To augment the interaction between the two polymers, we modified the surfaces of the PE films by dielectric barrier discharge (DBD) plasma before chitosan coating. After that the plasma-treated PE films were immersed in chitosan acetate solutions with different concentrations of chitosan. The optimum plasma treatment time was 10 s as determined from contact angle measurement. Effect of the plasma treatment on the surface roughness of the PE films was investigated by atomic force microscope (AFM) while the occurrence of polar functional groups was observed by X-ray photoelectron spectroscope (XPS) and Fourier transformed infrared spectroscope (FTIR). It was found that the surface roughness as well as the occurrence of oxygen-containing functional groups (i.e., C═O, C-O, and -OH) of the plasma-treated PE films increased from those of the untreated one, indicating that the DBD plasma enhanced hydrophilicity of the PE films. The amounts of chitosan coated on the PE films were determined after washing the coated films in water for several number of washing cycles prior to detection of the chitosan content by the Kjaldahl method. The amounts of chitosan coated on the PE films were constant after washing for three times and the chitosan-coated PE films exhibited appreciable antibacterial activity against Escherichia coli and Staphylococcus aureus. Hence, the obtained chitosan-coated PE films could be a promising candidate for antibacterial food packaging.

  15. Effect of nanoclay on the properties of low density polyethylene/linear low density polyethylene/thermoplastic starch blend films.

    PubMed

    Sabetzadeh, Maryam; Bagheri, Rouhollah; Masoomi, Mahmood

    2016-05-05

    The aim of this work is to study effect of nanoclay (Cloisite(®)15A) on morphology and properties of low-density polyethylene/linear low-density polyethylene/thermoplastic starch (LDPE/LLDPE/TPS) blend films. LDPE/LLDPE blend (70/30wt/wt) containing 15wt.% TPS in the presence of PE-grafted maleic anhydride (PE-g-MA, 3wt.%) with 1, 3 and 5phr of nanoclay are compounded in a twin-screw extruder and then film blown using a blowing machine. Nanocomposites with intercalated structures are obtained, based on the X-ray diffraction (XRD) and transmission electron microscopy (TEM) studies. However, some exfoliated single platelets in the samples are also observable. Scanning electron microscopic (SEM) images confirm the ability of both exfoliated nanoclay and PE-g-MA to reduce the size of TPS domains and deform their particles within the PE matrices. As the nanoclay content increases from 1 to 5phr, the tensile strength, tear resistance and impact strength of the films increase, whereas a slight decrease in the elongation at break is observed. The film samples with 5phr nanoclay possess the required packaging properties, as specified by ASTM D4635. These films provide desired optical transparency and surface roughness which are more attractive for packaging applications.

  16. Polyethylene terephthalate thin films; a luminescence study

    NASA Astrophysics Data System (ADS)

    Carmona-Téllez, S.; Alarcón-Flores, G.; Meza-Rocha, A.; Zaleta-Alejandre, E.; Aguilar-Futis, M.; Murrieta S, H.; Falcony, C.

    2015-04-01

    Polyethylene Terephthalate (PET) films doped with Rare Earths (RE3+) have been deposited on glass by spray pyrolysis technique at 240 °C, using recycled PET and (RE3+) chlorides as precursors. Cerium, terbium, dysprosium and europium were used as dopants materials, these dopants normally produce luminescent emissions at 450, 545, 573 and 612 nm respectively; the doped films also have light emissions at blue, green, yellow and red respectively. All RE3+ characteristic emissions were observed at naked eyes. Every deposited films show a high transmission in the visible range (close 80% T), films surfaces are pretty soft and homogeneous. Films thickness is around 3 μm.

  17. 76 FR 54791 - Polyethylene Terephthalate (PET) Film From Korea

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-09-02

    ... COMMISSION Polyethylene Terephthalate (PET) Film From Korea Determination On the basis of the record \\1... antidumping duty order on polyethylene terephthalate (PET) film from Korea would not be likely to lead to... contained in USITC Publication 4254 (August 2011), entitled Polyethylene Terephthalate (PET) Film from...

  18. Cell-compatible properties of calcium carbonates and hydroxyapatite deposited on ultrathin poly(vinyl alcohol)-coated polyethylene films.

    PubMed

    Serizawa, Takeshi; Tateishi, Taishi; Akashi, Mitsuru

    2003-01-01

    Poly(vinyl alcohol) (PVA) was coated onto polyethylene (PE) films by a repetitive adsorption and drying process, and then the PVA-coated PE films were alternately immersed into aqueous solutions of Ca2+ and CO3(2-) ions (alternate soaking cycles), to deposit calcium carbonate (CaCO3) onto the films. The PVA coating was essential for the CaCO3 deposition. The amount of CaCO3 deposited increased with an increasing number of cycles. Scanning electron microscopic observations and attenuated total reflection spectra revealed the presence of both calcite and aragonite as the crystal structures of CaCO3 on the film. L929 fibroblast cells adhered and proliferated on these CaCO3-deposited PE films, as well as the hydroxyapatite-coated PE films previously prepared. It was found that the PVA coating and the subsequent deposition of calcium salts on certain films facilitated cell compatibility.

  19. 76 FR 8770 - Polyethylene Terephthalate (Pet) Film From Korea

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-02-15

    ... From the Federal Register Online via the Government Publishing Office ] INTERNATIONAL TRADE COMMISSION Polyethylene Terephthalate (Pet) Film From Korea AGENCY: United States International Trade... full five-year review concerning the antidumping duty order on polyethylene terephthalate (PET)...

  20. Nonlinear viscoelastic characterization of thin polyethylene film

    NASA Technical Reports Server (NTRS)

    Wilbeck, J. S.

    1981-01-01

    In order to understand the state of stress and strain in a typical balloon fabricated from thin polyethylene film, experiment data in the literature reviewed. It was determined that the film behaves as a nonlinear viscoelasticity material and should be characterized accordingly. A simple uniaxial, nonlinear viscoelastic model was developed for predicting stress given a certain strain history. The simple model showed good qualitative agreement with results of constant rate, uniaxial accurately predicting stresses for cyclic strain histories typical of balloon flights. A program was outlined which will result in the development of a more complex nonlinear viscoelastic model.

  1. 78 FR 9668 - Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Final Results of Antidumping Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-02-11

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Final Results... polyethylene terephthalate film (PET Film) from Taiwan.\\1\\ This review covers two respondents, Shinkong.... \\1\\ See Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Preliminary Results...

  2. 77 FR 73428 - Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic of China...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-12-10

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic... the antidumping duty order on polyethylene terephthalate film, sheet, and strip (``PET film'') from... Duty Administrative Review: Polyethylene Terephthalate Film, Sheet, and Strip from the...

  3. Bio-based biodegradable film to replace the standard polyethylene cover for silage conservation.

    PubMed

    Borreani, Giorgio; Tabacco, Ernesto

    2015-01-01

    The research was aimed at studying whether the polyethylene (PE) film currently used to cover maize silage could be replaced with bio-based biodegradable films, and at determining the effects on the fermentative and microbiological quality of the resulting silages in laboratory silo conditions. Biodegradable plastic film made in 2 different formulations, MB1 and MB2, was compared with a conventional 120-μm-thick PE film. A whole maize crop was chopped; ensiled in MB1, MB2, and PE plastic bags, 12.5kg of fresh weight per bag; and opened after 170d of conservation. At silo opening, the microbial and fermentative quality of the silage was analyzed in the uppermost layer (0 to 50mm from the surface) and in the whole mass of the silo. All the silages were well fermented with little differences in fermentative quality between the treatments, although differences in the mold count and aerobic stability were observed in trial 1 for the MB1 silage. These results have shown the possibility of successfully developing a biodegradable cover for silage for up to 6mo after ensiling. The MB2 film allowed a good silage quality to be obtained even in the uppermost part of the silage close to the plastic film up to 170d of conservation, with similar results to those obtained with the PE film. The promising results of this experiment indicate that the development of new degradable materials to cover silage till 6mo after ensiling could be possible.

  4. 78 FR 2365 - Polyethylene Terephthalate Film, Sheet and Strip From India: Partial Rescission of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-01-11

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Partial... request an administrative review of the antidumping duty (AD) order on polyethylene terephthalate film... Polyester Film, Inc., SKC, Inc., and Toray Plastics (America), Inc. \\3\\ See Polyethylene Terephthalate...

  5. 78 FR 48147 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-08-07

    ...] Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary Results of Countervailing Duty... the countervailing duty (CVD) order on polyethylene terephthalate film, sheet and strip (PET film..., the products covered are all gauges of raw, pretreated, or primed polyethylene terephthalate...

  6. 75 FR 81570 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary Results of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-28

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary... semiannual new shipper review (NSR) under the antidumping duty order on polyethylene terephthalate film... Fair Value and Antidumping Duty Order: Polyethylene Terephthalate Film, Sheet, and Strip from India,...

  7. 77 FR 9892 - Polyethylene Terephthalate Film, Sheet and Strip from India: Preliminary Intent to Rescind...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-02-21

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip from India: Preliminary... polyethylene terephthalate film, sheet and strip from India covering the period January 1, 2010, through... Vacmet and Polypacks. See Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission,...

  8. 78 FR 48651 - Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan; Preliminary Results of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-08-09

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan; Preliminary... conducting an administrative review of the antidumping duty order on polyethylene terephthalate film, sheet... preliminary results. \\1\\ See Polyethylene Terephthalate Film, Sheet and Strip from Taiwan: Partial...

  9. 76 FR 76948 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Final Results of Countervailing...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-12-09

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From India: Final Results...) issued the preliminary results of the administrative review of polyethylene terephthalate film, sheet and... Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary Results of Countervailing...

  10. 77 FR 19634 - Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission of Countervailing Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-04-02

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission of... an administrative review of the countervailing duty (CVD) order on polyethylene terephthalate film... administrative review with respect to Vacmet and Polypacks. See Polyethylene Terephthalate Film, Sheet and...

  11. Effect of environmental conditions on the permeability of high density polyethylene film to fumigant vapors.

    PubMed

    Papiernik, Sharon K; Yates, Scott R

    2002-04-15

    Soil fumigation in greenhouses or agricultural fields often includes tarping the soil surface with polyethylene (PE) films to contain the fumigant in the soil and reduce emissions to the atmosphere. Previous research has demonstrated that PE films are permeable to methyl bromide and other fumigant compounds. In these experiments, the effect of temperature, fumigant mixtures, condensed water, and field aging on the permeability of high-density polyethylene (HDPE) was determined. Mass transfer coefficients (h, a measure of permeability) of the fumigants methyl bromide, 1,3-dichloropropene, propargyl bromide, and chloropicrin across HDPE films were determined. In these studies, temperature and HDPE film type had the largest impact on the h of fumigant compounds across HDPE films. Other factors investigated, including fumigant mixtures, condensed water on the film, and field aging of UV-stabilized film, did not have a significant impact on h. The results of these experiments suggest that the permeability of an intact piece of an agricultural film will increase with increasing temperature but is relatively constant despite changes in other environmental conditions.

  12. Effect of ethanol on the sorption of four targeted wine volatile compounds in a polyethylene film.

    PubMed

    Peyches-Bach, Aurelie; Dombre, Clara; Moutounet, Michel; Peyron, Stephane; Chalier, Pascale

    2012-07-11

    The objectives of this study were to demonstrate that the presence of ethanol in a solution containing two esters and two aromatic alcohols has several consequences on the sorption of these compounds into polyethylene (PE) film. First, sorption of ethanol into the PE film occurred at the same time as water and reached 8 kg m(-3) using 12% v/v of ethanol. This sorption was associated with an increase in PE crystallinity, which may have prevented the sorption of volatile compounds despite their strong affinity with PE film, as evaluated by Hansen solubility parameters. Moreover, increasing the ethanol concentration increased the solubility of the four volatile compounds. In the case of aromatic alcohols, the sorption was decreased in the presence of ethanol as expected. In the case of esters, as their hydrolysis was substantial in the presence of water, the consequence was a higher sorption into the PE film in the presence of ethanol than in its absence. Nevertheless, the sorption also depended on the concentration of ethanol and the heterogeneity of the ethanol-water mixture as well as the presence of other volatile compounds, as in the case of 4-ethylphenol. In conditions simulating wine packaging, losses of volatile compound by sorption and by permeation estimated after only 5 days of contact varied between 0.08 and 25% for 2-phenylethanol and ethyl hexanoate, respectively.

  13. Viscoplastic tearing of polyethylene thin film

    NASA Astrophysics Data System (ADS)

    Hegyi, Dezso; Pellegrino, Sergio

    2015-05-01

    Recent advances in noncontact strain measurement techniques and large-strain constitutive modeling of the linear low-density polyethylene film used in NASA superpressure balloons StratoFilm 420 are combined to provide a novel measurement technique for the tear propagation critical value of the J-integral. Previously these measurements required complex test configurations and procedures. It is found that the critical value of the J-integral increases by approximately 50 % when the strain rate is decreased from 1.33×10-4 s-1 to 1.33×10-5 s-1. It is shown that there is good correlation between measurements made on uniaxially loaded dogbone samples and circular diaphragms loaded by pressure, both with a 2-mm-wide slit in the middle. This result indicates that more extensive studies of strain-rate dependence may be made with the simpler, uniaxial test configuration.

  14. A flexible transparent Ag-NC@PE film as a cut-and-paste SERS substrate for rapid in situ detection of organic pollutants.

    PubMed

    Zhou, Ningning; Meng, Guowen; Huang, Zhulin; Ke, Yan; Zhou, Qitao; Hu, Xiaoye

    2016-10-21

    This report presents a simple and inexpensive fabrication approach to a flexible transparent composite film as a "cut-and-paste" surface-enhanced Raman scattering (SERS) substrate for in situ detection of organic pollutants. First, a self-assembled monolayer of Ag-nanocubes (Ag-NCs) is obtained at the air/water interface. Then, the Ag-NC monolayer is retrieved onto a flexible transparent polyethylene (PE) film to achieve an Ag-NC@PE composite film as a flexible SERS substrate. As the Ag-NCs in the monolayer are closely and uniformly packed on the PE film, the Ag-NC@PE composite film shows high SERS-activity with good signal homogeneity and reproducibility. Furthermore, the flexible transparent Ag-NC@PE composite film is "cut into" small pieces and directly "pasted" onto contaminated fruits for in situ SERS detection, as a result 10 nM thiram, 1 μM 4-polychlorinated biphenyl and 10 nM methyl parathion contaminants on oranges are detected, respectively. Therefore the Ag-NC@PE composite film is an inexpensive and effective SERS substrate for rapid in situ detection of organic pollutants in aqueous solutions, on fruits and other solid objects.

  15. Microbial dynamics during aerobic exposure of corn silage stored under oxygen barrier or polyethylene films.

    PubMed

    Dolci, Paola; Tabacco, Ernesto; Cocolin, Luca; Borreani, Giorgio

    2011-11-01

    The aims of this study were to compare the effects of sealing forage corn with a new oxygen barrier film with those obtained by using a conventional polyethylene film. This comparison was made during both ensilage and subsequent exposure of silage to air and included chemical, microbiological, and molecular (DNA and RNA) assessments. The forage was inoculated with a mixture of Lactobacillus buchneri, Lactobacillus plantarum, and Enterococcus faecium and ensiled in polyethylene (PE) and oxygen barrier (OB) plastic bags. The oxygen permeability of the PE and OB films was 1,480 and 70 cm³ m⁻² per 24 h at 23°C, respectively. The silages were sampled after 110 days of ensilage and after 2, 5, 7, 9, and 14 days of air exposure and analyzed for fermentation characteristics, conventional microbial enumeration, and bacterial and fungal community fingerprinting via PCR-denaturing gradient gel electrophoresis (DGGE) and reverse transcription (RT)-PCR-DGGE. The yeast counts in the PE and OB silages were 3.12 and 1.17 log₁₀ CFU g⁻¹, respectively, with corresponding aerobic stabilities of 65 and 152 h. Acetobacter pasteurianus was present at both the DNA and RNA levels in the PE silage samples after 2 days of air exposure, whereas it was found only after 7 days in the OB silages. RT-PCR-DGGE revealed the activity of Aspergillus fumigatus in the PE samples from the day 7 of air exposure, whereas it appeared only after 14 days in the OB silages. It has been shown that the use of an oxygen barrier film can ensure a longer shelf life of silage after aerobic exposure.

  16. 77 FR 73010 - Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab Emirates; Preliminary...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-12-07

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab... (the Department) is conducting an administrative review of the antidumping duty order on polyethylene...- treated, or primed polyethylene terephthalate film, whether extruded or co-extruded. Excluded...

  17. 75 FR 6634 - Polyethylene Terephthalate Film, Sheet, and Strip from India: Final Results of Countervailing...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-02-10

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip from India: Final Results... the preliminary results of administrative review of the countervailing duty order on polyethylene..., 2007. See Polyethylene Terephthalate Film, Sheet, and Strip from India: Preliminary Results...

  18. 76 FR 76365 - Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab Emirates: Preliminary...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-12-07

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab...) is conducting an administrative review of the antidumping duty order on polyethylene terephthalate... from the UAE. See Polyethylene Terephthalate Film, Sheet, and Strip From Brazil, the People's...

  19. 78 FR 50029 - Polyethylene Terephthalate Film, Sheet and Strip From Brazil: Preliminary Results of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-08-16

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From Brazil: Preliminary... Commerce (the Department) initiated an administrative review of the antidumping duty order on polyethylene... Preliminary Results of the Antidumping Duty Administrative Review of Polyethylene Terephthalate Film,...

  20. Creep behavior of 6 micrometer linear low density polyethylene film

    NASA Technical Reports Server (NTRS)

    Simpson, J. M.; Schur, W. W.

    1993-01-01

    Creep tests were performed to provide material characteristics for a 6.4-micron polyethylene film used to construct high altitude balloons. Results suggest simple power law relationships are adequate for stresses below about 4.83 MPa.

  1. 78 FR 47276 - Polyethylene Terephthalate (PET) Film, Sheet, and Strip From India: Final Results of the...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-08-05

    ... International Trade Administration Polyethylene Terephthalate (PET) Film, Sheet, and Strip From India: Final... of the countervailing duty order on polyethylene terephthalate (PET) film, sheet, and strip (``PET film'') from India. The Department finds that revocation of this countervailing duty order...

  2. Adsorption of Polyethylene from Solution onto Starch Film Surfaces

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Starch films were prepared by jet cooking aqueous dispersions of high-amylose starch and then allowing the jet cooked dispersions to air-dry on Teflon surfaces. When the starch films were immersed in 1 % solutions of PE in 1-dodecanol, dodecane and xylene at 120º C and the solutions were allowed to...

  3. Effect of POLYURETHANE/NANO-SiO2 Composites Coating on Thermo-Mechanical Properties of Polyethylene Film

    NASA Astrophysics Data System (ADS)

    Ching, Yern Chee; Yaacob, Iskandar Idris

    2011-06-01

    Polyethylene (PE) film was coated with polyurethane/nanosilica composite layer using rod Mayer process. The polyurethane/nanosilica system was prepared by dispersing nanosilica powder into solvent borne polyurethane (PU) binder under vigorous stirring. The silica nanoparticle used has an average diameter of 16 nm, and their weight fraction were varied from 0 % to 14 %. Two different thicknesses of the PU/nanosilica coating layer were fabricated which were about 4 μm and 8 μm. The structure and thermal mechanical features of the nanocomposite coated PE film were characterized by scanning electron microscope (SEM), dynamic mechanical analyzer (DMA), thermogravimetric analyzer (TGA) as well as tensile tests. The results showed that thin layer coating of the PU/nanosilica composite reduced tensile strength of PE substrate slightly. However, the nanocomposite coating of up to 8 μm reduced the elongation % of PE substrate significantly. PU/nanosilica composite coating layer increased the tensile modulus and stiffness of PE substrate. There was no influence of the PU/nanosilica composite coating to the thermal degradation rate of PE film.

  4. 78 FR 9670 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Final Results of Administrative...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-02-11

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From India: Final Results... order on polyethylene terephthalate film (PET Film) from India.\\1\\ This review covers three respondents... the ``Final Results of Review'' section below. \\1\\ See Polyethylene Terephthalate Film, Sheet,...

  5. 76 FR 9745 - Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Final Results of Antidumping Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-02-22

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Final Results...) published the preliminary results of administrative review of the antidumping duty order on polyethylene terephthalate film (PET Film) from Taiwan. See Polyethylene Terephthalate Film, Sheet, and Strip From...

  6. 75 FR 10758 - Polyethylene Terephthalate Film, Sheet and Strip from India: Initiation of Antidumping Duty and...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-03-09

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip from India: Initiation of...) orders on Polyethylene Terephthalate Film, Sheet and Strip (PET Film) from India. The Department... Less Than Fair Value and Antidumping Duty Order: Polyethylene Terephthalate Film, Sheet, and Strip...

  7. 75 FR 49902 - Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Preliminary Results of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-08-16

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Preliminary... ] administrative review of the antidumping duty order on polyethylene terephthalate film, sheet, and strip (PET...: Polyethylene Terephthalate Film, Sheet, and Strip (PET Film) from Taiwan, 67 FR 46566 (July 1, 2002). On July...

  8. 78 FR 77649 - Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab Emirates; Preliminary...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-12-24

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab... antidumping duty order on polyethylene terephthalate film, sheet, and strip (PET Film) from the United Arab... primed polyethylene terephthalate film, whether extruded or co-extruded. Excluded are metallized...

  9. 76 FR 39855 - Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, in Part, of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-07

    ... From the Federal Register Online via the Government Publishing Office ] DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, in... administrative review of the antidumping duty order on polyethylene terephthalate film, sheet and strip...

  10. 76 FR 39855 - Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, in Part, of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-07

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, in... administrative review of the countervailing duty order on polyethylene terephthalate film, sheet and strip...

  11. 76 FR 58248 - Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, In Part, of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-09-20

    ... From the Federal Register Online via the Government Publishing Office ] DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, In... (CVD) order on polyethylene terephthalate film, sheet and strip from India covering the period...

  12. 78 FR 2369 - Polyethylene Terephthalate Film, Sheet and Strip From India: Partial Rescission of Countervailing...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-01-11

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Partial... (CVD) order on polyethylene terephthalate film, sheet and strip from India covering the period...

  13. 76 FR 18156 - Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-04-01

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of... polyethylene terephthalate film, sheet and strip from India covering the period January 1, 2009,...

  14. 76 FR 76941 - Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Final Results of Antidumping Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-12-09

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Final Results... administrative review of the antidumping duty order on polyethylene terephthalate film, sheet and strip (PET Film... are listed in the ``Final Results of Review'' section, below. \\1\\ See Polyethylene Terephthalate...

  15. 75 FR 78968 - Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab Emirates: Preliminary...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-17

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab...) is conducting an administrative review of the antidumping duty order on polyethylene terephthalate... on PET Film from the UAE. See Polyethylene Terephthalate Film, Sheet, and Strip From Brazil,...

  16. 76 FR 30908 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Final Results of Antidumping Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-05-27

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From India: Final Results...) issued the preliminary results of the new shipper review of polyethylene terephthalate film, sheet and... INFORMATION: Background Since the issuance of Polyethylene Terephthalate Film, Sheet, and Strip From...

  17. 76 FR 30910 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Final Results of Countervailing...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-05-27

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From India: Final Results...) issued the preliminary results of the new shipper review of polyethylene terephthalate film, sheet and... Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary Results of Countervailing Duty...

  18. 75 FR 65450 - Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-10-25

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of... the antidumping duty order on polyethylene terephthalate film, sheet and strip from India for the period July 1, 2009 through December 31, 2009. See Polyethylene Terephthalate Film, Sheet and Strip...

  19. 77 FR 14501 - Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-03-12

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of...) order on polyethylene terephthalate film, sheet and strip from India covering the period July 1, 2010... respect to Vacmet and Polypacks on September 20, 2011. See Polyethylene Terephthalate Film, Sheet...

  20. 76 FR 75870 - Polyethylene Terephthalate Film, Sheet, and Strip From Korea: Notice of Rescission of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-12-05

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Korea: Notice of... polyethylene terephthalate film, sheet, ] and strip from Korea on July 28, 2011.\\1\\ This review covers one... the antidumping duty order on polyethylene terephthalate film, sheet, and strip from Korea with...

  1. 78 FR 67113 - Polyethylene Terephthalate Film, Sheet and Strip From India and Taiwan: Preliminary Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-11-08

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India and Taiwan...'') initiated the second sunset review of the antidumping duty orders on Polyethylene Terephthalate Film, Sheet... Value and Antidumping Duty Order: Polyethylene Terephthalate Film, Sheet, and Strip from India, 67...

  2. 76 FR 48122 - Polyethylene Terephthalate Film, Sheet, and Strip From Brazil: Preliminary Results of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-08-08

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Brazil: Preliminary... administrative review of the antidumping duty order on polyethylene terephthalate film, sheet, and strip (PET... Department published the antidumping duty order on PET film from Brazil. See Polyethylene Terephthalate...

  3. 76 FR 57715 - Polyethylene Terephthalate Film, Sheet, and Strip From the Republic of Korea: Revocation of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-09-16

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the Republic of Korea... its third sunset review of the antidumping duty order on polyethylene terephthalate film, sheet, and... existing antidumping duty order on polyethylene terephthalate film, sheet, and strip from the Republic...

  4. 77 FR 3730 - Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, in Part, of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-01-25

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, in... administrative review of the antidumping duty (AD) order on polyethylene terephthalate film, sheet and strip from... respect to Vacmet and Polypacks on September 20, 2011. See Polyethylene Terephthalate Film, Sheet...

  5. 78 FR 79400 - Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic of China: Initiation...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-12-30

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic... a request for a new shipper review of the antidumping duty order on polyethylene terephthalate film.... SUPPLEMENTARY INFORMATION: Background The antidumping duty order on polyethylene terephthalate film, sheet,...

  6. 78 FR 35245 - Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic of China: Final...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-06-12

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic... review of the antidumping duty order on polyethylene terephthalate film, sheet, and strip (``PET film... review (``POR'') is November 1, 2010, through October 31, 2011. \\1\\ See Polyethylene Terephthalate...

  7. Solvent effect in the polyethylene recovery from multilayer postconsumer aseptic packaging.

    PubMed

    Cervantes-Reyes, Alejandro; Núñez-Pineda, Alejandra; Barrera-Díaz, Carlos; Varela-Guerrero, Víctor; Martínez-Barrera, Gonzalo; Cuevas-Yañez, Erick

    2015-04-01

    Polyethylene films were separated and recovered from polyethylene-aluminum composites derived from recycling multilayer postconsumer aseptic packaging. A brief study about the separation process by dissolving PE-aluminum (PE-Al) composites into a series of organic solvents with a combination of time and temperature is presented. Through this procedure, 56% polyethylene is recovered from this kind of composites in optimized conditions. DSC and TGA studies were performed to determine the thermal stability of recovered polyethylene films and to establish a comparison with a PE reference commercial product, demonstrating that recovered polyethylene films kept their thermal properties.

  8. 75 FR 53711 - Polyethylene Terephthalate (PET) Film From Korea

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-09-01

    ... [Federal Register Volume 75, Number 169 (Wednesday, September 1, 2010)] [Notices] [Pages 53711-53714] [FR Doc No: 2010-21366] INTERNATIONAL TRADE COMMISSION [Investigation No. 731-TA-459 (Third Review)] Polyethylene Terephthalate (PET) Film From Korea AGENCY: United States International...

  9. Covalent attachment of lactase to low-density polyethylene films.

    PubMed

    Goddard, J M; Talbert, J N; Hotchkiss, J H

    2007-01-01

    Polymer films to which bioactive compounds such as enzymes are covalently attached offer potential for in-package processing of food. Beta-galactosidase (lactase) was covalently attached to surface-functionalized low-density polyethylene films. A two-step wet chemical functionalization introduced 15.7 nmol/cm2 primary amines to the film surface. Contact angle, dye assays, X-ray photoelectron spectroscopy, and appropriate protein assays were used to characterize changes in film surface chemistry after each step in the process of attachment. Glutaraldehyde was used to covalently attach lactase to the surface at a density of 6.0 microg protein per cm2 via reductive amination. The bond between the covalently attached lactase and the functionalized polyethylene withstood heat treatment in the presence of an ionic denaturant with 74% enzyme retention, suggesting that migration of the enzyme into the food product would be unlikely. The resulting polyethylene had an enzyme activity of 0.020 lactase units (LU)/cm2 (approximately 4500 LU/g). These data suggest that enzymes that may have applications in foods can be covalently attached to inert polymer surfaces, retain significant activity, and thus have potential as a nonmigratory active packaging materials.

  10. 76 FR 42113 - Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic of China: Extension...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-18

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic... of polyethylene terephthalate film, sheet, and strip (``PET film'') from the People's Republic of... notice of initiation of the second administrative review of the antidumping duty order on PET film...

  11. 76 FR 61085 - Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic of China: Extension...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-10-03

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic... review of polyethylene terephthalate film, sheet, and strip (``PET film'') from the People's Republic of... notice of initiation of the second administrative review of the antidumping duty order on PET film...

  12. 75 FR 40784 - Polyethylene Terephthalate Film, Sheet, and Strip from the Republic of Korea: Preliminary Results...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-07-14

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip from the Republic of Korea... administrative review of the antidumping duty order on polyethylene terephthalate film, sheet and strip (PET film... the antidumping duty order on PET film from Korea. See Antidumping or Countervailing Duty...

  13. 76 FR 47540 - Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Preliminary Results of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-08-05

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Preliminary... administrative review of the antidumping duty order on polyethylene terephthalate film, sheet, and strip (PET... Determination of Sales at Less Than Fair Value and Antidumping Duty Order: Polyethylene Terephthalate...

  14. 77 FR 46687 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary Results of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-08-06

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary... administrative review of the antidumping duty order on polyethylene terephthalate film, sheet, and strip (PET... Determination of Sales at Less Than Fair Value and Antidumping Duty Order: Polyethylene Terephthalate...

  15. 77 FR 1668 - Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, in Part, of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-01-11

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, in... administrative review of the countervailing duty (CVD) order on polyethylene terephthalate film, sheet and strip... administrative review with respect to Vacmet and Polypacks on September 20, 2011. See Polyethylene...

  16. 75 FR 75172 - Polyethylene Terephthalate Film, Sheet, and Strip From Brazil: Final Results of Antidumping Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-02

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Brazil: Final Results...) published the preliminary results of the administrative review of the antidumping duty order on polyethylene... covering PET film from Brazil and invited interested parties to comment. See Polyethylene...

  17. An assessment of athrombogenic properties of electret polyethylene film.

    PubMed

    Lowkis, B; Szymonowicz, M

    1998-01-01

    This paper shows the results of an investigation into the effect of an electric charge on blood platelet adhesion. All of the experiments were made on a polyethylene film. The electrets were formed using the electron beam method. The assessment of the electret effect on blood platelet adhesion was performed microscopically. It was found out that an electric charge plays a major role in the process of adhesion of blood morphological elements.

  18. Radiation-induced graft copolymerization of binary monomer mixture containing acrylonitrile onto polyethylene films

    NASA Astrophysics Data System (ADS)

    Choi, Seong-Ho; Nho, Young Chang

    2000-04-01

    Graft copolymerization of acrylonitrile (AN)/acrylic acid (AA), acrylonitrile (AN)/methacrylic acid (MA), and acrylonitrile (AN)/glycidyl methacrylate (GMA) onto pre-irradiated polyethylene (PE) films were studied. The effect of reaction conditions such as solvents, additives, and monomer composition on the grafting yields was investigated. The extent of grafting was found to increase with increasing sulfuric acid concentration when sulfuric acid as an additive was added to the grafting solution. In AN/AA mixture, the proportion of acrylonitrile in the copolymer increased with an increasing AN component in feed monomers. On the other hand, in AN/MA mixture, acrylonitrile component in copolymer was very slight in spite of the increase AN component in feed monomers. In the AN/GMA mixture, the proportion of acrylonitrile in the copolymer increased with increasing acrylonitrile component in AN/GMA feed monomer.

  19. 78 FR 42105 - Polyethylene Terephthalate Film, Sheet, and Strip From India and Taiwan; Notice of Commission...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-07-15

    ... From the Federal Register Online via the Government Publishing Office INTERNATIONAL TRADE COMMISSION Polyethylene Terephthalate Film, Sheet, and Strip From India and Taiwan; Notice of Commission... countervailing duty order on polyethylene terephthalate film, sheet, and strip (``PET'' film) from India and...

  20. 76 FR 47558 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-08-05

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary... administrative review under the countervailing duty (CVD) order on polyethylene terephthalate film, sheet and... Register the CVD order on PET Film from India. See Notice of Countervailing Duty Order:...

  1. 77 FR 31833 - Polyethylene Terephthalate Film, Sheet, and Strip From Brazil: Notice of Rescission of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-05-30

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Brazil: Notice of... polyethylene terephthalate film, sheet, and strip (PET Film) from Brazil for the period November 1,...

  2. 76 FR 71512 - Polyethylene Terephthalate Film, Sheet, and Strip From Korea: Final Results of Antidumping Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-11-18

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Korea: Final Results... of the antidumping duty order on polyethylene terephthalate film, sheet, and strip (PET film) from Korea, covering the June 1, 2009, to May 31, 2010, period of review (POR).\\1\\ \\1\\ See...

  3. 75 FR 80457 - Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-22

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of... terephthalate film, sheet and strip from India for the period July 1, 2009, through December 31, 2009. See Polyethylene Terephthalate Film, Sheet and Strip from India: Initiation of Antidumping Duty and...

  4. 75 FR 69400 - Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-11-12

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of... terephthalate film, sheet and strip from India for the period January 1, 2009, through December 31, 2009. See Polyethylene Terephthalate Film, Sheet and Strip from India: Initiation of Antidumping Duty and...

  5. Electron beam induced modification of poly(ethylene terephthalate) films

    NASA Astrophysics Data System (ADS)

    Vasiljeva, I. V.; Mjakin, S. V.; Makarov, A. V.; Krasovsky, A. N.; Varlamov, A. V.

    2006-10-01

    Electron beam processing of poly(ethylene terephthalate) (PET) films is found to promote significant changes in the melting heat, intrinsic viscosity and polymer film-liquid (water, isooctane and toluene) boundary surface tension. These properties are featured with several maximums depending on the absorbed dose and correlating with the modification of PET surface functionality. Studies using adsorption of acid-base indicators and IR-spectroscopy revealed that the increase of PET surface hydrophilicity is determined by the oxidation of methylene and methyne groups. Electron beam treatment of PET films on the surface of N-vinylpyrrolidone aqueous solution provided graft copolymerization with this comonomer at optimum process parameters (energy 700 keV, current 1 mA, absorbed dose 50 kGy).

  6. Recovery of polypropylene and polyethylene from packaging plastic wastes without contamination of chlorinated plastic films by the combination process of wet gravity separation and ozonation.

    PubMed

    Reddy, Mallampati Srinivasa; Okuda, Tetsuji; Nakai, Satoshi; Nishijima, Wataru; Okada, Mitsumasa

    2011-08-01

    Wet gravity separation technique has been regularly practiced to separate the polypropylene (PP) and polyethylene (PE) (light plastic films) from chlorinated plastic films (CP films) (heavy plastic films). The CP films including poly vinyl chloride (PVC) and poly vinylidene chloride (PVDC) would float in water even though its density is more than 1.0g/cm(3). This is because films are twisted in which air is sometimes entrapped inside the twisted CP films in real existing recycling plant. The present research improves the current process in separating the PP and PE from plastic packaging waste (PPW), by reducing entrapped air and by increasing the hydrophilicity of the CP films surface with ozonation. The present research also measures the hydrophilicity of the CP films. In ozonation process mixing of artificial films up to 10min reduces the contact angle from 78° to 62°, and also increases the hydrophilicity of CP films. The previous studies also performed show that the artificial PVDC films easily settle down by the same. The effect of ozonation after the wet gravity separation on light PPW films obtained from an actual PPW recycling plant was also evaluated. Although actual light PPW films contained 1.3% of CP films however in present case all the CP films were removed from the PPW films as a settled fraction in the combination process of ozonation and wet gravity separation. The combination process of ozonation and wet gravity separation is the more beneficial process in recovering of high purity PP and PE films from the PPW films.

  7. 75 FR 70901 - Polyethylene Terephthalate Film, Sheet, and Strip From the Republic of Korea: Final Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-11-19

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the Republic of Korea... polyethylene terephthalate film, sheet and strip (PET film) from the Republic of Korea (Korea). See Polyethylene Terephthalate Film, Sheet, and Strip from the Republic of Korea: Preliminary Results...

  8. 78 FR 29700 - Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab Emirates: Final Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-05-21

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab... duty order on polyethylene terephthalate film (PET Film) from the United Arab Emirates.\\1\\ This review... ``Final Results of Review.'' \\1\\ See Polyethylene Terephthalate Film, Sheet, and Strip from the...

  9. 76 FR 22867 - Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab Emirates: Final Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-04-25

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab... duty order on polyethylene terephthalate film (PET Film) from the United Arab Emirates. This review... preliminary results, the following events have taken place. See Polyethylene Terephthalate Film, Sheet,...

  10. Influence of different factors on the destruction of films based on polylactic acid and oxidized polyethylene

    NASA Astrophysics Data System (ADS)

    Podzorova, M. V.; Tertyshnaya, Yu. V.; Pantyukhov, P. V.; Shibryaeva, L. S.; Popov, A. A.; Nikolaeva, S.

    2016-11-01

    Influence of different environmental factors on the degradation of film samples based on polylactic acid and low density polyethylene with the addition of oxidized polyethylene was studied in this work. Different methods were used to find the relationship between degradation and ultraviolet, moisture, oxygen. It was found that the addition of oxidized polyethylene, used as a model of recycled polyethylene, promotes the degradation of blends.

  11. 76 FR 13128 - Polyethylene Terephthalate Film, Sheet, and Strip (PET Film) From Taiwan: Extension of Time Limit...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-03-10

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip (PET Film) From Taiwan: Extension of Time Limit for the Preliminary Results of the Antidumping Duty Administrative Review...

  12. 76 FR 72676 - Polyethylene Terephthalate Film, Sheet, and Strip From Brazil: Final Results of Antidumping Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-11-25

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Brazil: Final Results...) published the preliminary results of the administrative review of the antidumping duty order on polyethylene... duty order covering PET film from Brazil and invited interested parties to comment. See...

  13. 75 FR 14423 - Polyethylene Terephthalate Film, Sheet and Strip from Taiwan: Extension of Time Limit for...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-03-25

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip from Taiwan: Extension of... polyethylene terephthalate film, sheet and strip from Taiwan for the period July 1, 2008 through June 30, 2009... time that the Department conducted an administrative review of the antidumping order on...

  14. 76 FR 58244 - Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, in Part, of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-09-20

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, in...) order on polyethylene terephthalate film, sheet and strip from India covering the period July 1,...

  15. 76 FR 45508 - Polyethylene Terephthalate Film, Sheet and Strip From the United Arab Emirates: Extension of Time...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-29

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From the United Arab... of the antidumping duty order on polyethylene terephthalate film, sheet and strip from the...

  16. Antibacterial performance of alginic acid coating on polyethylene film.

    PubMed

    Karbassi, Elika; Asadinezhad, Ahmad; Lehocký, Marian; Humpolíček, Petr; Vesel, Alenka; Novák, Igor; Sáha, Petr

    2014-08-21

    Alginic acid coated polyethylene films were examined in terms of surface properties and bacteriostatic performance against two most representative bacterial strains, that is, Escherichia coli and Staphylococcus aureus. Microwave plasma treatment followed by brush formation in vapor state from three distinguished precursors (allylalcohol, allylamine, hydroxyethyl methacrylate) was carried out to deposit alginic acid on the substrate. Surface analyses via various techniques established that alginic acid was immobilized onto the surface where grafting (brush) chemistry influenced the amount of alginic acid coated. Moreover, alginic acid was found to be capable of bacterial growth inhibition which itself was significantly affected by the brush type. The polyanionic character of alginic acid as a carbohydrate polymer was assumed to play the pivotal role in antibacterial activity. The cell wall composition of two bacterial strains along with the substrates physicochemical properties accounted for different levels of bacteriostatic performance.

  17. Characterization and inventory of PBDD/F emissions from deca-BDE, polyethylene (PE) and metal blends during the pyrolysis process.

    PubMed

    Mei, Jun; Wang, Xiuji; Xiao, Xiao; Cai, Ying; Tang, Yuhui; Chen, Pei

    2017-02-16

    The thermal treatment of waste electrical and electronic equipment (WEEE) is regarded as the largest potential contributor to the environmental release of polybrominated dibenzo-p-dioxins/dibenzofurans (PBDD/Fs). Herein, the pyrolysis of decabromodiphenyl ether (deca-BDE), polyethylene (PE) and metal blends was conducted to investigate the emission characteristics of PBDD/Fs at different thermal treatment conditions. The total yield of polybrominated dibenzo-p-dioxins (PBDDs) was less than that of polybrominated dibenzofurans (PBDFs) during the pyrolysis of the PE matrix and metal blends. 2,3,7,8-TBDF and 1,2,3,7,8-PBDF were the dominant congeners emitted from the pyrolysis. Temperature, presence of oxygen and type of added metal were the critical influencing factors for the PBDD/F formation rates and speciation in the pyrolysis process.

  18. The role of UHMW-PE in microporous PE separators

    SciTech Connect

    Wang, L.C.; Harvey, M.K.; Stein, H.L.; Scheunemann, U.

    1997-12-01

    Microporous PE separators have gained large popularity in the lead acid battery industry, particularly in SLI (Starting, Lighting and Ignition) Automotive Applications. The PE (Polyethylene) in battery separator is actually UHMW-PE (Ultra High Molecular Weight Polyethylene). UHMW-PE has a molecular weight more than ten times that of conventional HDPE (High Density Polyethylene). This paper gives an overview of the UHMW-PE`s contributions to the PE battery separator process, assembly, and performance, in comparison to other conventional separators, such as PVC (Polyvinyl Chloride), cellulose, and glass fiber.

  19. Poly(2-hydroxyethyl methacrylate) (PHEMA) grafted polyethylene/polypropylene (PE/PP) nonwoven fabric by γ-initiation: Synthesis, characterization and benefits of RAFT mediation

    NASA Astrophysics Data System (ADS)

    Kodama, Yasko; Barsbay, Murat; Güven, Olgun

    2014-12-01

    Polyethylene/polypropylene (PE/PP) nonwoven fabrics were functionalized by γ-initiated RAFT mediated grafting of 2-hydroxyethyl methacrylate (HEMA), and the characterization of the grafted samples was carried out using various techniques. FTIR and XPS analysis showed an increase in the oxygenated content till a certain degree of grafting. The results implied a grafting process following the concept of ‘front mechanism’. The initial grafting occurred on the topmost surface layer, and then moved further into the bulk of the polymer matrix. Reversible addition-fragmentation chain transfer (RAFT) mediated grafting yielded a better controlled grafting when compared to those obtained in conventional grafting.

  20. 77 FR 76456 - Polyethylene Terephthalate Film, Sheet and Strip from Taiwan: Partial Rescission of the...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-12-28

    ... [Federal Register Volume 77, Number 249 (Friday, December 28, 2012)] [Notices] [Page 76456] [FR Doc No: 2012-31320] DEPARTMENT OF COMMERCE International Trade Administration [A-583-837] Polyethylene... an administrative review of the antidumping duty (AD) order on polyethylene terephthalate film,...

  1. 76 FR 18519 - Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Amended Final Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-04-04

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Amended Final... Department) published the final results of the antidumping duty administrative review of polyethylene...), pursuant to section 751(h) of the Tariff Act of 1930, as amended (the Act). \\1\\ See...

  2. 78 FR 14266 - Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Notice of Correction to the Final...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-03-05

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Notice of... antidumping duty order on polyethylene terephthalate film, sheet, and strip (PET Film) from Taiwan.\\1\\ The... contained a clerical error, in that it identified an incorrect case number associated with PET Film...

  3. 77 FR 18206 - Polyethylene Terephthalate Film, Sheet, and Strip (PET Film) From Taiwan: Extension of Time Limit...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-03-27

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip (PET Film) From Taiwan... Department) initiated the administrative review regarding the antidumping duty order on PET Film from Taiwan... it is not practicable to complete the preliminary results of the administrative review of PET...

  4. Influence of high doses γ-irradiation on oxygen permeability of linear low-density polyethylene and cast polypropylene films

    NASA Astrophysics Data System (ADS)

    Klepac, Damir; Ščetar, Mario; Baranović, Goran; Galić, Kata; Valić, Srećko

    2014-04-01

    Linear low density polyethylene (PE-LLD) and cast polypropylene (PPcast) films were irradiated in a 60Co γ-source. The total irradiation dose varied from 0 kGy (unirradiated samples) to 200 kGy. Oxygen transport was investigated by a manometric method and the structural changes were studied by differential scanning calorimetry (DSC) and Fourier transform infrared spectroscopy (FTIR). Free radicals decay as a function of time was monitored by electron spin resonance (ESR) spectroscopy. The results show that the γ-irradiation reduces oxygen permeability coefficient in both films. The reduction was associated with an increase in crystallinity. DSC thermograms revealed a decrease in PPcast melting point with increasing irradiation dose, indicating higher degradation compared to PE-LLD. The observed peak in FTIR spectra for both samples at 1716 cm-1 corresponds to the stretching of the carbonyl and carboxylic groups which arise from the reaction of oxygen with the free radicals produced in the polymer matrix as a result of irradiation.

  5. Surface modification on polyethylene terephthalate films with 2-methacryloyloxyethyl phosphorylcholine.

    PubMed

    Zheng, Zhiwen; Ren, Li; Zhai, Zhichen; Wang, Yingjun; Hang, Fei

    2013-07-01

    In this study, the surface of polyethylene terephthalate (PET) was modified to improve the protein and cell adhesion behavior with low temperature ammonia plasma treatment followed by 2-methacryloyloxyethyl phosphorylcholine (MPC) grafting. The x-ray photoelectron spectroscopy (XPS) results showed that the -COO(-), -N-C=O and -P-O-H groups were successfully incorporated onto the sample surface after MPC grafting. Furthermore, formation of new bonds, -N= and N-H on the sample surface grafted with MPC was recorded by Fourier transform infrared spectroscopy (FTIR). A large number of spherical particles at submicron to nanometer scale were also observed on the surface by atomic force microscopy (AFM). The cell adhesion experiments on PET film surfaces were evaluated and the highly hydrophilic surfaces could not promote cell adhesion and spreading. All results achieved in this study have clearly indicated that the method combining low temperature ammonia plasma treatment and MPC grafting is an effective way of producing a suitably hydrophilic PET surface with the capability of weakening the protein adsorption greatly.

  6. Influence of polyethylene glycol-300 addition on nanostructured lead sulfide thin films properties

    NASA Astrophysics Data System (ADS)

    Kaci, S.; Keffous, A.; Trari, M.; Menari, H.; Manseri, A.; Mahmoudi, B.; Guerbous, L.

    2010-09-01

    The concentration of polyethylene glycol-300 was found to play a crucial role in the formation of nanoparticles in PbS-chemical bath deposition process. We report here an endeavor to set up a relation between the variation of lead sulfide (PbS) nanocrystalline thin film properties, grown by (CBD) process at room temperature on corning glass and Si(100) substrates, with amount fluctuations of polyethylene glycol-300 in the solution. The transmittance of the films, for a fixed reaction time, increased up to ˜ 80% with the increase of % polyethylene glycol-300 in the solution, indicating the formation of very thin films due to the decrease of reaction rate with the increase of the concentration of polyethylene glycol-300. The optical band gaps were found to strongly rely on the composition of the bath deposition and increase with the increase of the polyethylene glycol-300 amount in the solution. Particle sizes between 2.8 and 8.7 nm were obtained by varying the % of polyethylene glycol-300 from 0.2 to 1.5. The concentration of polyethylene glycol-300 not only affects the reaction rate but also the morphology of the obtained films. PbS nanoparticles were found to be oriented preferentially along the < 200> plane. The absorption shifts towards short wavelength indicating a blue-shifting as a consequence of quantum confinement.

  7. Determination of microplastic polyethylene (PE) and polypropylene (PP) in environmental samples using thermal analysis (TGA-DSC).

    PubMed

    Majewsky, Marius; Bitter, Hajo; Eiche, Elisabeth; Horn, Harald

    2016-10-15

    Microplastics are increasingly detected in the environment and the consequences on water resources and ecosystems are not clear to date. The present study provides a cost-effective and straightforward method to determine the mass concentrations of polymer types using thermal analysis. Characteristic endothermic phase transition temperatures were determined for seven plastic polymer types using TGA-DSC. Based on that, extracts from wastewater samples were analyzed. Results showed that among the studied polymers, only PE and PP could be clearly identified, while the phase transition signals of the other polymers largely overlap each other. Subsequently, calibration curves were run for PE and PP for qualitative measurements. 240 and 1540mg/m(3) of solid material (12µm to 1mm) was extracted from two wastewater effluent samples of a municipal WWTP of which 34% (81mg/m(3)) and 17% (257mg/m(3)) could be assigned to PE, while PP was not detected in any of the samples. The presented application of TGA-DSC provides a complementary or alternative method to FT-IR analyses for the determination of PE and PP in environmental samples.

  8. 78 FR 19524 - Polyethylene Terephthalate Film, Sheet, and Strip From India and Taiwan; Institution of Five-Year...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-04-01

    ... From the Federal Register Online via the Government Publishing Office INTERNATIONAL TRADE COMMISSION Polyethylene Terephthalate Film, Sheet, and Strip From India and Taiwan; Institution of Five-Year... polyethylene terephthalate film, sheet, and strip (``PET film'') from India and the antidumping duty orders...

  9. 77 FR 20357 - Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab Emirates: Final Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-04-04

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab... duty order on polyethylene terephthalate film (PET Film) from the United Arab Emirates.\\1\\ This review... final dumping margins, see the ``Final Results of Review'' section below. \\1\\ See...

  10. 76 FR 12937 - Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for Final...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-03-09

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of... under the antidumping duty order on polyethylene terephthalate film, sheet and strip from India for SRF... Film, Sheet and Strip from India: Preliminary Results of Antidumping Duty New Shipper Review, 75...

  11. 76 FR 12938 - Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for Final...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-03-09

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of... under the countervailing duty order on polyethylene terephthalate film, sheet and strip from India for... Terephthalate Film, Sheet, and Strip From India: Preliminary Results of Countervailing Duty New Shipper...

  12. Reconstruction of the Interface of Oxidatively Functionalized Polyethylene (PE-CO2H) and Derivatives on Heating. Revision.

    DTIC Science & Technology

    1987-03-01

    interfacial free energy. A slower process--probably driven simply by the entropy of dilution of the concentrated interfacial functionality into the polymer...itself reconstruct the interface: If reaction 4’tn the annydride had Drought the hydroxyl moiety up into the "qterpnase, then upon hydrolysis the...study the reconstruction of PE[dansyl] during heating: the fluorescence emission maximum and the quenching of fluorescence upon protonation of its

  13. Improvement in mechanical and barrier properties of polyethylene blown films using atomic layer deposition

    SciTech Connect

    Lee, Gyeong Beom; Hak Song, Seung; Wook Moon, Sung; Woo Kim, Jun; Hyung Shim, Joon; Choi, Byoung-Ho; Moo Heo, Young

    2014-01-15

    Recently, thin films deposited on polymer substrates have been widely utilized as encapsulation barriers in electronic applications such as flexible displays, packaging films, and organic light-emitting diodes. The barrier and mechanical properties of these films are critical aspects when using them for protecting the inner modules of electronic devices from environmental factors such as moisture, oxygen, and sunlight. In particular, polymers can be degraded or decomposed more easily than other materials under such environmental conditions. Therefore, polymer films can be deposited using thin functional materials; however, suitable deposition methods for polymers are scarce owing to many limitations such as low melting/glass transition temperature, thermal degradation, and oxidation. In this study, a thin alumina oxide film was deposited on a high-density polyethylene blown film by using atomic layer deposition. The mechanical and barrier properties of the alumina oxide film deposited on the polyethylene film were characterized by a microtensile test and water vapor transmission rate test. Process conditions such as process temperature, plasma surface treatment, and number of cycles were varied to ascertain the reliability of the thin alumina oxide film deposited on the high-density polyethylene blown film. The results showed that the barrier property of the deposited film improved upon the application of plasma surface treatment, and that its mechanical properties varied under different process conditions.

  14. 76 FR 18155 - Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-04-01

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of... terephthalate film, sheet and strip from India covering the period July 1, 2009, through June 30, 2010....

  15. Crystallization of Ethylene Vinyl Acetate (EVA) and Polyethylene (PE) /deuterated Polystyrene (dPS) Blends in Supercritical Carbon Dioxide (scCO2)

    NASA Astrophysics Data System (ADS)

    Pynn, Christopher; Ahdout, Payvand; Jerome, John; Wang, Yantian; Zaitsev, Vladimir; Soklov, Johnathan; Rafailovich, Miriam; Schwarz, Steven

    2006-03-01

    Thin films of EVA or PE and dPS were spun cast onto Si wafers and crystallized in supercritical carbon dioxide at pressures and temperatures corresponding to the density fluctuation ridge^1 or thermally annealed using standard protocols. The morphology composition and melting points of the films were studied using scanning force microscopy and imaging time-of-flight secondary ion mass spectrometry as function of film thickness and homopolymer concentration. The results showed that exposure to scCO2 produced highly crystalline films. Furthermore, in contrast to the thermally annealed films, the homopolymer was fully incorporated into the crystalline phase. The surface morphology of the films after crystallization showed either island or hole structure, depending on the relation between the film thickness and the lamellar height. Supported in part by the NSF-MRSEC program and by a grant from the SRC-NYS consortium. Reference: ^1 Koga T., Seo Y.S., Shin K., Zhang Y., Rafailovich M., Sokolov J., B. Chu, Satija, S.K. Macromolecules. Vol. 36. 2003: 5236- 5243.

  16. Photoelectric dye-coupled polyethylene film as a prototype of retinal prostheses.

    PubMed

    Uji, Akihito; Matsuo, Toshihiko; Ishimaru, Sanae; Kajiura, Akiko; Shimamura, Kaoru; Ohtsuki, Hiroshi; Dan-oh, Yasufumi; Suga, Sadaharu

    2005-01-01

    Photoelectric dyes, which absorb light and convert photon energy to electric potentials, have been previously shown to stimulate retinal neurons in culture. In this study, a photoelectric dye was coupled to a polyethylene film surface and tested in vitro using retinal tissues from chick embryos at the 12-day embryonic stage, at which time outer segments of retinal photoreceptor cells have not yet developed. Carboxyl moieties were introduced to a polyethylene film surface by fuming nitric acid, and then a photoelectric dye, 2-[2-[4-(dibutylamino)phenyl]ethenyl]-3-carboxymethylbenzothiazolium bromide, was coupled to the film through amide linkage. Intracellular calcium elevation was observed with Fluo-4 in retinal tissues placed on the dye-coupled polyethylene film, in contrast to retinal tissues which had no contact with the film. The response was inhibited by calcicludine, a voltage-gated calcium channel blocker, and also by extracellular calcium depletion. The photoelectric dye, coupled to the polyethylene film surface, absorbed light under a dissecting microscope and stimulated neurons in retinal tissues, showing that the dye-coupled film could be used as a prototype of retinal prostheses.

  17. Raman study of uniaxial deformation of single-crystal mats of ultrahigh molecular weight linear polyethylene

    NASA Astrophysics Data System (ADS)

    Zavgorodnev, Yu V.; Chvalun, S. N.; Nikolaeva, G. Yu; Sagitova, E. A.; Pashinin, P. P.; Gordeyev, S. A.; Prokhorov, K. A.

    2015-03-01

    We present for the first time a Raman spectroscopic study of the deformation process of solution-crystallized single-crystal mats of ultrahigh molecular weight linear polyethylene (UHMW PE). We study the deformed regions of the films, drawn only until the formation of the neck, and the films of much higher draw ratios, just before rupture starts. For comparison, we have also carried out Raman investigations of films produced by compression of UHMW PE powder. We have found that the uniaxial molecular orientation in the neck region of the single-crystal mat films develops more slowly as compared to the films, prepared by compression of the UHMW PE powder.

  18. In Situ deposition of YBCO high-T(sub c) superconducting thin films by MOCVD and PE-MOCVD

    NASA Technical Reports Server (NTRS)

    Zhao, J.; Noh, D. W.; Chern, C.; Li, Y. Q.; Norris, P.; Gallois, B.; Kear, B.

    1990-01-01

    Metalorganic Chemical Vapor Deposition (MOCVD) offers the advantages of a high degree of compositional control, adaptability for large scale production, and the potential for low temperature fabrication. The capability of operating at high oxygen partial pressure is particularly suitable for in situ formation of high temperature superconducting (HTSC) films. Yttrium barium copper oxide (YBCO) thin films having a sharp zero-resistance transition with T( sub c) greater than 90 K and Jc approx. 10 to the 4th power A on YSZ have been prepared, in situ, at a substrate temperature of about 800 C. Moreover, the ability to form oxide films at low temperature is very desirable for device applications of HTSC materials. Such a process would permit the deposition of high quality HTSC films with a smooth surface on a variety of substrates. Highly c-axis oriented, dense, scratch resistant, superconducting YBCO thin films with mirror-like surfaces have been prepared, in situ, at a reduced substrate temperature as low as 570 C by a remote microwave-plasma enhanced metalorganic chemical vapor deposition (PE-MOCVD) process. Nitrous oxide was used as a reactant gas to generate active oxidizing species. This process, for the first time, allows the formation of YBCO thin films with the orthorhombic superconducting phase in the as-deposited state. The as-deposited films grown by PE-MOCVD show attainment of zero resistance at 72 K with a transition width of about 5 K. MOCVD was carried out in a commercial production scale reactor with the capability of uniform deposition over 100 sq cm per growth run. Preliminary results indicate that PE-MOCVD is a very attractive thin film deposition process for superconducting device technology.

  19. In-situ deposition of YBCO high-Tc superconducting thin films by MOCVD and PE-MOCVD

    NASA Technical Reports Server (NTRS)

    Zhao, J.; Noh, D. W.; Chern, C.; Li, Y. Q.; Norris, P. E.; Kear, B.; Gallois, B.

    1991-01-01

    Metal-Organic Chemical Vapor Deposition (MOCVD) offers the advantages of a high degree of compositional control, adaptability for large scale production, and the potential for low temperature fabrication. The capability of operating at high oxygen partial pressure is particularly suitable for in situ formation of high temperature superconducting (HTSC) films. Yttrium barium copper oxide (YBCO) thin films having a sharp zero-resistance transition with T(sub c) greater than 90 K and J(sub c) of approximately 10(exp 4) A on YSZ have been prepared, in situ, at a substrate temperature of about 800 C. Moreover, the ability to form oxide films at low temperature is very desirable for device applications of HTSC materials. Such a process would permit the deposition of high quality HTSC films with a smooth surface on a variety of substrates. Highly c-axis oriented, dense, scratch resistant, superconducting YBCO thin films with mirror-like surfaces have been prepared, in situ, at a reduced substrate temperature as low as 570 C by a remote microwave-plasma enhanced metal-organic chemical vapor deposition (PE-MOCVD) process. Nitrous oxide was used as a reactant gas to generate active oxidizing species. This process, for the first time, allows the formation of YBCO thin films with the orthorhombic superconducting phase in the as-deposited state. The as-deposited films grown by PE-MOCVD show attainment of zero resistance at 72 K with a transition width of about 5 K. MOCVD was carried out in a commercial production scale reactor with the capability of uniform deposition over 100 sq cm per growth run. Preliminary results indicate that PE-MOCVD is a very attractive thin film deposition process for superconducting device technology.

  20. Radiation synthesis of acrylamide/N,N-(dimethylamino) ethyl methacrylate grafted onto low density polyethylene films

    NASA Astrophysics Data System (ADS)

    Abdel Ghaffar, A. M.

    2011-02-01

    Radiation-induced graft copolymerization of acrylamide/N,N-(dimethylamino) ethyl methacrylate (AAm/DMAEMA) onto low density polyethylene films was carried out. The effect of grafting conditions such as solvent type and comonomer composition were studied. Characterization of the prepared films was investigated by Fourier transform infrared. Some selected properties such as thermal stability and swelling behavior were determined. It was found that grafting efficiency, swelling behavior and thermal stability increased with increasing DMAEMA content. Scanning electron microscopy was used for predicting the change in surface morphology via the grafted films. The improvement in properties of the prepared films make it possible to use them in some practical applications.

  1. 75 FR 79336 - Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-20

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for Preliminary Results of Countervailing Duty New Shipper Review AGENCY: Import Administration, International Trade...

  2. 78 FR 45512 - Polyethylene Terephthalate Film from India and Taiwan: Extension of Time Limits for Preliminary...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-07-29

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film from India and Taiwan: Extension of Time Limits for Preliminary and Final Results of the Second Antidumping Duty Sunset Reviews AGENCY: Import Administration, International...

  3. Langmuir films of dipalmitoyl phosphatidylethanolamine grafted poly(ethylene glycol). In-situ evidence of surface aggregation at the air-water interface.

    PubMed

    Clop, Eduardo M; Corvalán, Natalia A; Perillo, María A

    2016-12-01

    The molecular packing-dependent interfacial organization of polyethylene glycol grafted dipalmitoylphosphatidylethanolamine (PE-PEGs) Langmuir films was studied. The PEG chains covered a wide molecular mass range (350, 1000 and 5000Da). In surface pressure-area (π-A), isotherms PE-PEG(1000) and PE-PEG(5000) showed transitions (midpoints at πm,t1∼11mN/m, "t1"), which appeared as a long non-horizontal line region. Thus, t1 cannot be considered a first-order phase transition but may reflect a transition within the polymer, comprising its desorption from the air-water interface and compaction upon compression. This is supported by the increase in the νs(C-O-C) PM-IRRAS signal intensity and the increasing surface potentials at maximal compression, which reflect thicker polymeric layers. Furthermore, changes in hydrocarbon chain (HC) packing and tilt with respect to the surface led to reorientation in the PO2(-) group upon compression, indicated by the inversion of the νasym(PO2(-)) PM-IRRAS signal around t1. The absence of a t1 in PE-PEG(350) supports the requisite of a critical polymer chain length for this transition to occur. In-situ epifluorescence microscopy revealed 2D-domain-like structures in PE-PEG(1000) and PE-PEG(5000) around t1, possibly associated with gelation/dehydration of the polymeric layer and appearing at decreasing π as the polymeric tail became longer. Another transition, t2, appearing in PE-PEG(350) and PE-PEG(1000) at πm,t2=29.4 and 34.8mN/m, respectively, was associated with HC condensation and was impaired in PE-PEG(5000) due to steric hindrance imposed by the large size of its polymer moiety. Two critical lengths of polymer chains were found, one of which allowed the onset of polymeric-tail gelation and the other limited HC compaction.

  4. Evidence of polyethylene biodegradation by bacterial strains from the guts of plastic-eating waxworms.

    PubMed

    Yang, Jun; Yang, Yu; Wu, Wei-Min; Zhao, Jiao; Jiang, Lei

    2014-12-02

    Polyethylene (PE) has been considered nonbiodegradable for decades. Although the biodegradation of PE by bacterial cultures has been occasionally described, valid evidence of PE biodegradation has remained limited in the literature. We found that waxworms, or Indian mealmoths (the larvae of Plodia interpunctella), were capable of chewing and eating PE films. Two bacterial strains capable of degrading PE were isolated from this worm's gut, Enterobacter asburiae YT1 and Bacillus sp. YP1. Over a 28-day incubation period of the two strains on PE films, viable biofilms formed, and the PE films' hydrophobicity decreased. Obvious damage, including pits and cavities (0.3-0.4 μm in depth), was observed on the surfaces of the PE films using scanning electron microscopy (SEM) and atomic force microscopy (AFM). The formation of carbonyl groups was verified using X-ray photoelectron spectroscopy (XPS) and microattenuated total reflectance/Fourier transform infrared (micro-ATR/FTIR) imaging microscope. Suspension cultures of YT1 and YP1 (10(8) cells/mL) were able to degrade approximately 6.1 ± 0.3% and 10.7 ± 0.2% of the PE films (100 mg), respectively, over a 60-day incubation period. The molecular weights of the residual PE films were lower, and the release of 12 water-soluble daughter products was also detected. The results demonstrated the presence of PE-degrading bacteria in the guts of waxworms and provided promising evidence for the biodegradation of PE in the environment.

  5. ToF-SIMS imaging of PE/PP polymer using multivariate analysis

    NASA Astrophysics Data System (ADS)

    Miyasaka, Toyomitsu; Ikemoto, Takashi; Kohno, Teiichiro

    2008-12-01

    The distribution of polyethylene (PE) and polypropylene (PP) in PE/PP blended-polymer film was determined by applying principal components analysis (PCA) and multivariate curve resolution (MCR) to time-of-flight secondary ion mass spectroscopy (ToF-SIMS) imaging, together with preprocessing by pixel binning, normalization, and autoscaling to increase image contrast by reducing topographic and charge-distribution effects. The PE/PP distribution was confirmed by MVA conducted on the image data over static limit. The MCR score with normalized-autoscaling was found to give the PE/PP distribution distinctly.

  6. Engineering functional nanothin multilayers on food packaging: ice-nucleating polyethylene films.

    PubMed

    Gezgin, Zafer; Lee, Tung-Ching; Huang, Qingrong

    2013-05-29

    Polyethylene is the most prevalent plastic and is commonly used as a packaging material. Despite its common use, there are not many studies on imparting functionalities to those films which can make them more desirable for frozen food packaging. Here, commercial low-density polyethylene (LDPE) films were oxidized by UV-ozone (UVO) treatment to obtain a negatively charged hydrophilic surface to allow fabrication of functional multilayers. An increase in hydrophilicity was observed when films were exposed to UVO for 4 min and longer. Thin multilayers were formed by dipping the UVO-treated films into biopolymer solutions, and extracellular ice nucleators (ECINs) were immobilized onto the film surface to form a functional top layer. Polyelectrolyte adsorption was studied and confirmed on silicon wafers by measuring the water contact angles of the layers and investigating the surface morphology via atomic force microscopy. An up to 4-5 °C increase in ice nucleation temperatures and an up to 10 min decrease in freezing times were observed with high-purity deionized water samples frozen in ECIN-coated LDPE films. Films retained their ice nucleation activity up to 50 freeze-thaw cycles. Our results demonstrate the potential of using ECIN-coated polymer films for frozen food application.

  7. Polyethylene/silver-nanofiber composites: A material for antibacterial films.

    PubMed

    Zapata, Paula A; Larrea, Maialen; Tamayo, Laura; Rabagliati, Franco M; Azócar, M Ignacio; Páez, Maritza

    2016-12-01

    Silver nanofibers (Ag-Nfbs)~80nm in diameter were synthesized by hydrothermal treatment. The nanofibers (3 and 5wt%) were added in the initial feed together with the catalytic system. Polymerizations in an ethylene atmosphere were performed, yielding PE nanocomposites in situ with 3 and 5wt% content of Ag-Nfbs. The antibacterial effect of the silver-nanofiber composites was evaluated after incubation of Escherichia coli ATCC 25923 for 8h on their surface. Bacterial viability tests showed that the silver-nanofiber composites inhibited the growth of Escherichia coli ATCC 25923 by 88 and 56%. This behavior is attributed to increased silver ions release from the nanocomposite. TEM analysis showed that the antibacterial effect is associated with membrane disruption but not with changes in shape.

  8. Radiation-induced grafting of diallyldimethylammonium chloride onto acrylic acid grafted polyethylene

    NASA Astrophysics Data System (ADS)

    Francis, Sanju; Dhanawade, B. R.; Mitra, D.; Varshney, Lalit; Sabharwal, Sunil

    2009-01-01

    Diallyldimethylammonium chloride (DADMAC) was grafted onto polyethylene (PE) films by a double grafting procedure. The PE film was initially modified by grafting acrylic acid (AA), through a mutual irradiation method. AA-g-PE film, thus obtained was subjected to subsequent radiation grafting reaction of DADMAC, to give a DADMAC-g-AA-g-PE film having a comb-type structure. The influence of different conditions, such as the extent of AA grafting, DADMAC concentration, absorbed dose and dose rate, on the grafting yield of DADMAC was investigated. A maximum DADMAC grafting of 30% was achieved. The equilibrium degree of swelling (EDS) of the grafted films were gravimetrically determined. TGA and FT-IR techniques were employed to characterize the grafted PE films.

  9. Diffuse Reflectance Spectroscopy of Hidden Objects, Part I: Interpretation of the Reflection-Absorption-Scattering Fractions in Near-Infrared (NIR) Spectra of Polyethylene Films.

    PubMed

    Pomerantsev, Alexey L; Rodionova, Oxana Ye; Skvortsov, Alexej N

    2017-01-01

    Investigation of a sample covered by an interfering layer is required in many fields, e.g., for process control, biochemical analysis, and many other applications. This study is based on the analysis of spectra collected by near-infrared (NIR) diffuse reflectance spectroscopy. Each spectrum is a composition of a useful, target spectrum and a spectrum of an interfering layer. To recover the target spectrum, we suggest using a new phenomenological approach, which employs the multivariate curve resolution (MCR) method. In general terms, the problem is very complex. We start with a specific problem of analyzing a system, which consists of several layers of polyethylene (PE) film and underlayer samples with known spectral properties. To separate information originating from PE layers and the target, we modify the system versus both the number of the PE layers as well as the reflectance properties of the target sample. We consider that the interfering spectrum of the layer can be modeled using three components, which can be tentatively called transmission, absorption, and scattering contributions. The novelty of our approach is that we do not remove the reflectance and scattering effects from the spectra, but study them in detail aiming to use this information to recover the target spectrum.

  10. Extruded films of blended chitosan, low density polyethylene and ethylene acrylic acid.

    PubMed

    Martínez-Camacho, A P; Cortez-Rocha, M O; Graciano-Verdugo, A Z; Rodríguez-Félix, F; Castillo-Ortega, M M; Burgos-Hernández, A; Ezquerra-Brauer, J M; Plascencia-Jatomea, M

    2013-01-16

    The obtaining of chitosan extruded films was possible by using low density polyethylene (LDPE) as a matrix polymer and ethylene-acrylic acid copolymer as an adhesive, in order to ensure adhesion in the interphase of the immiscible polymers. The obtained blend films were resistant; however, a reduction in the mechanical resistance was observed as chitosan concentration increased. The thermal stability of the films showed a certain grade of interaction between polymers as seen in FTIR spectra. The antifungal activity of the extruded films was assessed against Aspergillus niger and high inhibition percentages were observed, which may be mainly attributed to barrier properties of the extruded films and the limited oxygen availability, resulting in the inability of the fungi to grow. A low adherence of fungal spores to the material surface was observed, mainly in areas with chitosan clumps, which can serve as starting points for material degradation.

  11. Effect of ablation parameters on infrared pulsed laser deposition of poly(ethylene glycol) films

    NASA Astrophysics Data System (ADS)

    Bubb, Daniel M.; Papantonakis, M. R.; Toftmann, B.; Horwitz, J. S.; McGill, R. A.; Chrisey, D. B.; Haglund, R. F., Jr.

    2002-06-01

    Polymer thin films were deposited by laser ablation using infrared radiation both resonant (2.90, 3.40, 3.45, and 8.96 mum) and nonresonant (3.30, 3.92, and 4.17 mum) with vibrational modes in the starting material, polyethylene glycol. The chemical structure of the films was characterized by Fourier transform infrared spectroscopy, while the molecular weight distribution was investigated using gel permeation chromatography. The films deposited by resonant irradiation are superior to those deposited with nonresonant radiation with respect to both the chemical structure and the molecular weight distribution of the films. However, the molecular-weight distributions of films deposited at nonresonant infrared wavelengths show marked polymer fragmentation. Fluence and wavelength dependence studies show that the effects may be related to the degree of thermal confinement, and hence to the relative absorption strengths of the targeted vibrational modes.

  12. Crystallization studies of polyethylene -poly(ethylene glycol) graft copolymers

    NASA Astrophysics Data System (ADS)

    Mark, P. R.; Hovey, G. E.; Murthy, N. S.; Breitenkamp, K.; Kade, M.; Emerick, T.

    2006-03-01

    Structure and crystallization behavior of three copolymers obtained by grafting poly (ethylene glycol) (PEG) chains to polyethylene (PE) main chain was investigated by variable temperature x-ray diffraction and thermal analysis. The results show that PEG side chains and PE main chains crystallize into separate domains. This is especially true when grafted chains are long (50 and 100 repeat units), in which the PEG domains are same as in PEG homopolymer both in structure and in melting behavior. In the copolymer with shorter chains (25 repeat units), the PEG crystals are not distinct and melting is broad. The PEG domains can be dissolved in water or ethanol without altering the mechanical integrity of the film. PE crystallites in both samples are similar to that in PE homopolymer. For instance, the thermal expansion of the basal cell plane (a- and b-axes) of the PE domains agrees well with that of PE homopolymer over the entire temperature range from ambient to melt. However, the chain-axis dimension PE-lattice in the copolymer is shorter by ˜ 0.05 å and the basal dimensions are larger by ˜ 0.05 å. The changes in these dimensions due to the changes in the length of the grafted PEG chains were investigated.

  13. Supercritical fluid impregnation of polyethylene films, a new approach to studying equilibria in matrices; the hydrogen bonding of fluoroalcohols to (η 5-C 5Me 5)Ir(CO) 2 and the effect on CH activation

    NASA Astrophysics Data System (ADS)

    Cooper, Andrew I.; Kazarian, Sergei G.; Poliakoff, Martyn

    1993-04-01

    Polyethylene (PE) film is used as a matrix for studying temperature-dependent equilibria by IR spectroscopy; the film is impregnated with Cp*Ir(CO) 2 (Cp*=η 5-C 5Me 5) using supercritical CO 2 and subsequently saturated with HOR F (R F=(CF 3) 2CH or (CF 3) 3C). At 200 K, the equilibrium between Cp*Ip(CO) 2 and the hydrogen-bonded complex, Cp*Ir(CO) 2…HOR F, is frozen out and can be disturbed photochemically, because Cp*Ir(CO) 2 is more efficient than Cp*Ir(CO) 2…HOR F for CH activation of polyethylene.

  14. Functional polyethylene glycol derivatives nanostructured thin films synthesized by matrix-assisted pulsed laser evaporation

    NASA Astrophysics Data System (ADS)

    Cristescu, R.; Popescu, C.; Popescu, A.; Grigorescu, S.; Mihailescu, I. N.; Mihaiescu, D.; Gittard, S. D.; Narayan, R. J.; Buruiana, T.; Stamatin, I.; Chrisey, D. B.

    2009-09-01

    We report the thin film deposition by matrix-assisted pulsed laser evaporation (MAPLE) of a polymer conjugate with an hydrophilic sequence between metronidazole molecules that was covalently attached to both oligomer ends of carboxylate poly(ethylene glycol) (PEG 1.5-metronidazole). A pulsed KrF* excimer laser was used to deposit the drug-polymer composite films. Fourier transform infrared spectroscopy was used to demonstrate that MAPLE-transferred materials exhibited chemical properties similar to the starting materials. The dependence of the surface morphology on incident laser fluence is given.

  15. Preparation, characterization and antibacterial applications of ZnO-nanoparticles coated polyethylene films for food packaging.

    PubMed

    Tankhiwale, Rasika; Bajpai, S K

    2012-02-01

    The present work describes the preparation of ZnO nanoparticles loaded starch-coated polyethylene film. The presence of ZnO nanoparticles was confirmed by surface plasmon resonance (SPR), X-ray diffraction (XRD) studies and transmission electron microscopy (TEM). The ZnO loaded film was tested for its biocidal action against model bacteria Escherichia coli using zone inhibition and killing kinetics of bacterial growth methods. This newly developed material bears potential to be used as food packaging material to prevent food stuff from bacterial contamination.

  16. Structure and properties of polyethylene films used in heavy lift balloons

    NASA Technical Reports Server (NTRS)

    Khoury, F.; Crissman, J. M.; Fanconi, B. M.; Wagner, H. L.; Botz, L. H.

    1985-01-01

    The following features of five polyethylene films used by NASA in the construction of heavy lift balloons have been examined: molecular weight, molecular weight distribution, branching, melting behavior, density, surface texture, birefringence, orientation of crystalline regions, unlaxial deformation in the machine and transverse directions, and the effect of sample geometry and strain rate on deformation behavior. The goal of this exploratory study was to determine whether there are significant differences in any of the above mentioned features, or combination of features between the films. The acquisition of such information is a first step towards determining whether there are any specific correlations between film characteristics and the incidence of catastrophic failure of balloons during ascent through the troposphere. This exploratory study has resulted in the identification of similarities and differences between various features of the films.

  17. Chitosan/polyethylene glycol fumarate blend film: physical and antibacterial properties.

    PubMed

    Hashemi Doulabi, Azadehsadat; Mirzadeh, Hamid; Imani, Mohammad; Samadi, Nasrin

    2013-01-30

    The objective of this work was to prepare chitosan/polyethylene glycol fumarate (chitosan/PEGF) blend films as wound dressings and to evaluate the influence of composition ratio on the blending properties of the films. Blending chitosan with PEGF obviated the brittleness of neat chitosan film. Film topography performed by atomic force microscopy illustrated that blending could increase and control the surface roughness of the neat film. Their water vapor transmission rates were close to the range of 904-1447 g(-2)day(-1) found to be proper candidates for dressing the wounds with moderate exudates. Controlled water solubility, swelling, wettability and surface tension of the blend films were also evaluated. The blend films showed a powerful antibacterial activity against Pseudomonas aeruginosa and Staphylococcus aureus (Kill%>99.76 ± 0.16%). Physical properties as well as antibacterial activity assessments showed that among different compositions, the film comprising 80 wt% chitosan and 20 wt% PEGF is a suitable candidate for biomedical applications as a wound dressing material.

  18. Oxidation and biodegradation of polyethylene films containing pro-oxidantadditives: Synergistic effects of sunlight exposure, thermal aging and fungal biodegradation

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Synergistic effects of sunlight exposure, thermal aging and fungal biodegradation on the oxidation and biodegradation of linear low density poly (ethylene) PE-LLD films containing pro-oxidant were examined. To achieve oxidation and degradation, films were first exposed to the sunlight for 93 days du...

  19. Effects of polyethylene film wrap on cooler shrink and the microbial status of beef carcasses.

    PubMed

    Sampaio, Guilherme S L; Pflanzer-Júnior, Sérgio B; Roça, Roberto de O; Casagrande, Leandro; Bedeschi, Elaine A; Padovani, Carlos R; Miguel, Giulianna Z; Santos, Carolina T; Girão, Lucio V C; Miranda, Zander B; Franco, Robson M

    2015-02-01

    The present study evaluated the use of polyethylene film wrapping of beef half carcasses and its effects on cooler shrink, cooling characteristics and microbial status of the half carcasses. Film wrapping reduced cooler shrink by 55.2%, 43.1%, 36.0% and 30% after 24, 48, 72 and 96 h of cooling, respectively, compared to the unwrapped half carcasses, whereas the surface water activity showed no significant differences among the time periods. The wrapped half carcasses had a lower cooling rate and higher surface and internal temperatures. The highest values of the aerobic mesophiles, Staphylococcus aureus and Enterobacteriaceae were found in the half carcasses wrapped in film. No significant differences were found in the values of Escherichia coli. The polyethylene film was effective in reducing cooler shrink; however, it caused a delay in cooling, thereby enabling greater microbial occurrences and counts and impairing the hygienic and sanitary conditions of the carcasses, which may be an impediment to the practical application of this technology.

  20. Silicon-Germanium Films Deposited by Low Frequency PE CVD: Effect of H2 and Ar Dilution

    SciTech Connect

    Kosarev, A; Torres, A; Hernandez, Y; Ambrosio, R; Zuniga, C; Felter, T E; Asomoza, R R; Kudriavtsev, Y; Silva-Gonzalez, R; Gomez-Barojas, E; Ilinski, A; Abramov, A S

    2005-09-22

    We have studied structure and electrical properties of Si{sub 1-Y}Ge{sub Y}:H films deposited by low frequency PE CVD over the entire composition range from Y=0 to Y=1. The deposition rate of the films and their structural and electrical properties were measured for various ratios of the germane/silane feed gases and with and without dilution by Ar and by H{sub 2}. Structure and composition was studied by Auger electron spectroscopy (AES), secondary ion mass spectroscopy (SIMS) and Fourier transform infrared (FTIR) spectroscopy. Surface morphology was characterized by atomic force microscopy (AFM). We found: (1) The deposition rate increased with Y maximizing at Y=1 without dilution. (2) The relative rate of Ge and Si incorporation is affected by dilution. (3) Hydrogen preferentially bonds to silicon. (4) Hydrogen content decreases for increasing Y. In addition, optical measurements showed that as Y goes for 0 to 1, the Fermi level moves from mid gap to the conduction band edge, i.e. the films become more n-type. No correlation was found between the pre-exponential and the activation energy of conductivity. The behavior of the conductivity {gamma}-factor suggests a local minimum in the density of states at E {approx} 0.33 eV for the films grown with or without H-dilution and E {approx} 0.25 eV for the films with Ar dilution.

  1. Polyethylene films doped with nanophosphors for green house

    NASA Astrophysics Data System (ADS)

    Wilhelm, Justin; Hunter, David; Laudenslager, Tyler; Jia, Dongdong

    2006-10-01

    CaAl2O4:Eu^2+ and CaSCl:Eu^2+ nanophosphors are prepared by using a salted sol-gel method and a stabilized precipitation method respectively. The absorption of the CaAl2O4:Eu^2+ nanophosphor is in the UV to deep blue (200-400nm) range. Its emission is at 450 nm. The absorption of the CaSCl:Eu^2+ nanophosphor is broad from deep UV to orange. Its emission is at 670 nm which is exactly where photosynthesis absorption peak at. We are going to embed these nanophosphors in transparent polymer materials for a greenhouse. Using the colloidal suspension properties of Xanthan Gum, isolated from Xanthomonas campestris the desiccation resistance of the polymer will be utilized. Xanthan Gum observes low shear and high viscosity in aqueous solutions that will allow a thermal stabilization of a heavy metal phosphor-polymer colloid. The influence of pH on the system will be independent of the nucleation of the phosphor. By dispersing nanophosphors with Xanthan, transparent red and blue light enhance greenhouse film can be prepared.

  2. Electroluminescence and cathodoluminescence from polyethylene and polypropylene films: Spectra reconstruction from elementary components and underlying mechanisms

    SciTech Connect

    Qiao, B.; Teyssedre, G.; Laurent, C.

    2016-01-14

    The mechanisms of electroluminescence from large band gap polymers used as insulation in electric components are still under debate. It becomes important to unravel the underlying physics of the emission because of increasing thermo-electric stress and a possible relationship between electroluminescence and field withstand. We report herein on the cathodoluminescence spectra of polyethylene and polypropylene films as a way to uncover the nature of its contributions to electroluminescence emission. It is shown that spectra from the two materials are structured around four elementary components, each of them being associated with a specific process contributing to the overall emission with different weights depending on excitation conditions and on materials. The cathodoluminescence and electroluminescence spectra of each material are reconstructed from the four spectral components and their relative contribution are discussed. It is shown that electroluminescence from polyethylene and polypropylene has the same origin pointing towards generic mechanisms in both.

  3. Synthesis and characterization of electrically conductive polyethylene-supported graphene films

    PubMed Central

    2014-01-01

    We describe a simple mechanical approach for low-density polyethylene film coating by multilayer graphene. The technique is based on the exfoliation of nanocrystalline graphite (few-layer graphene) by application of shear stress and allows to obtain thin graphene layers on the plastic substrate. We report on the temperature dependence of electrical resistance behaviors in films of different thickness. The experimental results suggest that the semiconducting behavior observed at low temperature can be described in the framework of the Efros-Shklovskii variable-range-hopping model. The obtained films exhibit good electrical conductivity and transparency in the visible spectral region. PACS 72.80.Vp; 78.67.Wj; 78.66.Qn; 85.40.Hp PMID:25288910

  4. Effect of Oxidation on Localized Heat Generation and Dielectric Breakdown of Low-Density Polyethylene Film

    NASA Astrophysics Data System (ADS)

    Tsurimoto, Takao; Nagao, Masayuki; Kosaki, Masamitsu

    1995-12-01

    The effect of oxidation on localized heat generation and dielectric breakdown in low-density polyethylene (LDPE) film was studied by thermography. In the non-McKeown-type epoxy-free electrode system, localized heat generation of LDPE film leading to dielectric breakdown increased and breakdown strength decreased upon oxidation. In the McKeown-type specimen, however, the breakdown strength of oxidized LDPE film is higher than that of an unoxidized one. It is considered that enhancement of the thermal process is a major factor of breakdown in the epoxy-free electrode system and that homo-space charge and/or electron scattering effect is dominant in the McKeown type specimen.

  5. Electroless plating of nickel phosphorous on surface-modified poly(ethylene terephthalate) films

    NASA Astrophysics Data System (ADS)

    Domenech, S. C.; Lima, E.; Drago, V.; De Lima, J. C.; Borges, N. G.; Avila, A. O. V.; Soldi, V.

    2003-12-01

    Chemical surface preparation for Ni-P electroless metallization of poly(ethylene terephthalate) (PET) films without using Chromium-based chemicals, was studied. The applicability of this method was verified by a subsequent metallization process. Thermal analysis was conducted to observe the main thermal transitions and stability of the polymer and metallized films. Contact angle analysis was performed to assess the surface hydrophilicity so as to optimize the substrate preparation process. X-ray diffraction, EDAX and SEM analysis were used to understand the composition and morphology of the polymeric substrate and Ni-P coat growing process. Adherence strength, contact sheet resistivity and optical diffuse reflection were measured on the metallized films. The time of chemical etching affects the polymer surface hydrophilicity, polymer/metal adherence strength, surface resistance and optical diffuse reflection, while Ni coating morphology is controlled by the pH of the electroless bath. High wettability of the polymer surface, adherence strength of 800 N cm -2, high optical diffuse reflection and low surface resistivity of the Ni coating, were found for films etched for 60 min. Metallizations performed at pH 7.5 produce Ni-P coatings with 12.0 wt.% phosphorous content, which were amorphous and flexible. The contact sheet resistivity of the plated films is sensitive to roughness variations of the substrate. The method proposed in this work allows the production of metallized films appropriate for the fabrication of flexible circuits.

  6. New process for preparing complex-shaped dielectric film similar to Mylar. [Polyethylene terephthalate

    SciTech Connect

    Lagasse, R.R.; Kraynik, A.M.

    1982-02-01

    A new thermoforming/heat-treatment process yields complex-shaped dielectric film having electrical and shrinkage properties similar to those of flat Mylar film. This similarity should extend to other physical properties because the new process is directly analogous to the process used to prepare Mylar. Commercially available poly(ethylene terephthalate) film is formed into a cavity at approx. 110/sup 0/C and then heat treated at approx. 180/sup 0/C. A laboratory-scale forming apparatus has produced cylindrically shaped films having depth/diameter ratio approx. 1, a tapered wall-section, and variation in wall thickness of < 3X. Evaluation of other forming methods suggests that the production rate and thickness uniformity can be improved with existing technology. Thermal shrinkage at 150/sup 0/C, 1 kHz dielectric constant from -55 to +70/sup 0/C, leakage current at 1 kV, and breakdown voltage have been measured for both the complex-shaped film and Mylar. These comparative measurements indicate that the complex-shaped film could replace the flat Mylar dielectric currently used in energy-storage capacitors. A complex-shaped energy-storage capacitor could enhance safety in certain nuclear weapon applications by allowing strong-link devices in a firing set to be enclosed by a weak link.

  7. Acoustic study of a linear low-density polyethylene film after modification of the crystalline structure by heating.

    PubMed

    Tohmyoh, Hironori; Sakamoto, Yuhei

    2014-02-01

    We report on a hybrid microscopy technique that enables us to measure the acoustic properties of a thin polymer film together with an optical microscope image of the corresponding area. Linear low-density polyethylene films are heated to various temperatures and examined by the technique. Density of the film is increased by heating and its sound velocity is decreased compared with a film without heating. Also, spherulites can clearly be seen in the optical microscope image, supporting the thermal shrinkage of the film which can be detected by the present technique.

  8. Fabrication and anti-fouling properties of photochemically and thermally immobilized poly(ethylene oxide) and low molecular weight poly(ethylene glycol) thin films.

    PubMed

    Wang, Hui; Ren, Jin; Hlaing, Aye; Yan, Mingdi

    2011-02-01

    Poly(ethylene oxide) (PEO) and low molecular weight poly(ethylene glycol) (PEG) were covalently immobilized on silicon wafers and gold films by way of the CH insertion reaction of perfluorophenyl azides (PFPAs) by either photolysis or thermolysis. The immobilization does not require chemical derivatization of PEO or PEG, and polymers of different molecular weights were successfully attached to the substrate to give uniform films. Microarrays were also generated by printing polymer solutions on PFPA-functionalized wafer or Au slides followed by light activation. For low molecular weight PEG, the immobilization was highly dependent on the quality of the film deposited on the substrate. While the spin-coated and printed PEG showed poor immobilization efficiency, thermal treatment of the PEG melt on PFPA-functionalized surfaces resulted in excellent film quality, giving, for example, a grafting density of 9.2×10(-4)Å(-2) and an average distance between grafted chains of 33Å for PEG 20,000. The anti-fouling property of the films was evaluated by fluorescence microscopy and surface plasmon resonance imaging (SPRi). Low protein adsorption was observed on thermally-immobilized PEG whereas the photoimmobilized PEG showed increased protein adsorption. In addition, protein arrays were created using polystyrene (PS) and PEG based on the differential protein adsorption of the two polymers.

  9. Improved blood compatibility of poly(ethylene terephthalate) films modified with L-arginine.

    PubMed

    Liu, Yun; Chen, Jie-Rong; Yang, Yun; Wu, Feng

    2008-01-01

    In order to improve the blood compatibility of the commonly used blood-contacting biomaterial poly(ethylene terephthalate) (PET), in this study PET films were chemically modified with L-arginine (L-Arg) by a three-step-procedure using glutaraldehyde (GA) as a cross-linker. The composition and chemical structure of PET and its change with surface modification were examined by X-ray photoelectron spectroscopy (XPS) and attenuated total reflection Fourier transform infrared (ATR-FT-IR) spectroscopy, while the change in hydrophilicity was judged by water contact angles measurement. The result of water contact measurement indicated that the modified films became more hydrophilic than PET with the contact angle decreasing from 78.5 degrees for PET to 43.7 degrees for PET-Arg. The protein adsorption on the film surface was evaluated by bicinchoninic acid assay (BCA) method, and the result showed that the L-Arg-modified films decreased the amount of protein adsorption by about 25%. The in vitro blood compatibility such as platelet adhesion (observed by scanning electron microscopy) and thrombus formation was also investigated, and the results demonstrated that the L-Arg-modified films significantly suppressed platelet adhesion and aggregation and reduced the thrombus formation by about 67% compared with PET.

  10. Migration of polyisobutylene from polyethylene/polyisobutylene films into foods during domestic and microwave oven use.

    PubMed

    Castle, L; Nichol, J; Gilbert, J

    1992-01-01

    Migration of polyisobutylene from polyethylene/polyisobutylene film into foods has been studied in domestic applications such as wrapping of foods and reheating in a microwave oven. The results of these migration studies were obtained by direct measurement using newly developed analytical methods utilizing nuclear magnetic resonance (NMR) and infra-red (IR) spectroscopy as well as predictively from assessment of loss of polyisobutylene from the film. Total levels of polyisobutylene migration into cheese were found to be 8-10 mg/kg, into cake 1-5 mg/kg, and into sandwiches ranged from < 1 to 4 mg/kg. Reheating foods covered with film in the microwave oven, gave migration levels ranging from < 0.01 mg/kg for contact with steam only, up to 0.5 mg/kg for severe splashing of food onto the film and 4 mg/kg for reheated pizza. Migration of polyisobutylene was shown to be skewed towards the low molecular weight fraction of the additive. In typical films, the molecular weight range of polyisobutylene was shown to be 300-6000 daltons (95% limits) centred on 1300 daltons, whereas the additive that had migrated into cheese was found to range from 130-2200 daltons, centred on 520 daltons.

  11. Time-resolved detection of structural change in polyethylene films using mid-infrared laser pulses

    SciTech Connect

    Ageev, Eduard; Mizobata, Keisuke; Nakajima, Takashi Zen, Heishun; Kii, Toshiteru; Ohgaki, Hideaki

    2015-07-27

    Some of the vibrational modes of crystalline organic polymers are known to be sensitive to the structural change from the crystalline phase to the amorphous phase, and vice versa. Using a mid-infrared (mid-IR) pulse from a free-electron laser as a probe, we demonstrate the time-resolved detection of structural change in crystalline polymer (polyethylene) films upon laser heating by a Q-switched Nd:YAG laser. Transmittance of the resonant mid-IR pulse almost instantaneously changes before and after the Nd:YAG laser pulse if its fluence is sufficient to induce the structural change in the film. The developed technique would be useful to study the time-dependent dynamics of the structural change in various materials.

  12. Preparation and characterization of nonfouling polymer brushes on poly(ethylene terephthalate) film surfaces.

    PubMed

    Li, Jiehua; Tan, Dongsheng; Zhang, Xiaoqing; Tan, Hong; Ding, Mingming; Wan, Changxiu; Fu, Qiang

    2010-07-01

    In this study, a surface grafting of nonfouling poly(ethylene glycol) methyl ether acrylate (PEGMA) on poly(ethylene terephthalate) (PET) was carried out via surface-initiated atom-transfer radical polymerization (SI-ATRP) to improve hemocompatibility of polymer based biomaterials. To do this, the coupling agent with hydroxyl groups for the ATRP initiator was first anchored on the surface of PET films using photochemical method, and then these hydroxyl groups were esterified by bromoisobutyryl bromide, from which PET with various main chain lengths of PEGMA was prepared. The structures and properties of modified PET surfaces were investigated using water contact angle (WAC), ATR-FTIR, X-ray photoelectron spectroscopy (XPS) and Atomic force microscopy (AFM). The molecular weights of the free polymer from solution were determined by gel permeation chromatography (GPC). These results indicated that grafting of PEGMA on PET film is a simple way to change its surface properties. The protein adsorption resistance on the surfaces of PET was primarily evaluated by an enzyme-linked immunosorbent assay (ELISA). The result demonstrated that the protein adsorption could be well suppressed by poly(PEGMA) brush structure on the surface of PET. This work provides a new approach for polymers to enhance their biocompatibility.

  13. Patterning of Aluminium thin film on polyethylene terephthalate by multi-beam picosecond laser

    NASA Astrophysics Data System (ADS)

    Jin, Y.; Perrie, W.; Harris, P.; Allegre, O. J.; Abrams, K. J.; Dearden, G.

    2015-11-01

    High speed patterning of a 30 nm thick Aluminium thin film on a flexible Polyethylene Terephthalate substrate was demonstrated with the aid of Computer Generated Holograms (CGH's) applied to a phase only Spatial Light Modulator. Low fluence picosecond laser pulses minimise thermal damage to the sensitive substrate and thus clean, single and multi-beam, front side thin film removal is achieved with good edge quality. Interestingly, rear side ablation shows significant Al film delamination. Measured front and rear side ablation thresholds were Fth=0.20±0.01 J cm-2 and Fth=0.15±0.01 J cm-2 respectively. With laser repetition rate of 200 kHz and 8 diffractive spots, a film removal rate of R>0.5 cm2 s-1 was demonstrated during patterning with a fixed CGH and 5 W average laser power. The effective laser repetition rate was feff~1.3 MHz. The application of 30 stored CGH's switching up to 10 Hz was also synchronised with motion control, allowing dynamic large area multi-beam patterning which however, slows micro-fabrication.

  14. Metal adsorption of gamma-irradiated carboxymethyl cellulose/polyethylene oxide blend films

    NASA Astrophysics Data System (ADS)

    El-Naggar, Amal A.; Magida, M. M.; Ibrahim, Sayeda M.

    2016-03-01

    Blend films of different ratios of carboxymethyl cellulose (CMC)/polyethylene oxide (PEO) were prepared by the solution casting method. To investigate the effect of irradiation on all properties of prepared blend, it was exposed to different gamma irradiation doses (10, 20, and 30 kGy). Physical properties such as gel fraction (GF) (%) and swelling (SW) (%) were investigated. It was found that the GF (%) increases with increasing irradiation dose up to 20 kGy, while SW (%) decreases with an increase in the irradiation doses for all blend compositions. Moreover, the structural and mechanical properties of the prepared films were studied. The results of the mechanical properties obtained showed that there is an improvement in these properties with an increase in both CMC and irradiation dose up to 20 kGy. The efficiency of metal ions uptake was measured using a UV spectrophotometer. The prepared films showed good tendency to absorb and release metal ions from aqueous media. Thus, the CMC/PEO film can be used in agricultural domain.

  15. Modification and patterning of nanometer-thin poly(ethylene glycol) films by electron irradiation.

    PubMed

    Meyerbröker, Nikolaus; Zharnikov, Michael

    2013-06-12

    In this study, we analyzed the effect of electron irradiation on highly cross-linked and nanometer-thin poly(ethylene glycol) (PEG) films and, in combination with electron beam lithography (EBL), tested the possibility to prepare different patterns on their basis. Using several complementary spectroscopic techniques, we demonstrated that electron irradiation results in significant chemical modification and partial desorption of the PEG material. The initially well-defined films were progressively transformed in carbon-enriched and oxygen-depleted aliphatic layers with, presumably, still a high percentage of intermolecular cross-linking bonds. The modification of the films occurred very rapidly at low doses, slowed down at moderate doses, and exhibited a leveling off behavior at higher doses. On the basis of these results, we demonstrated the fabrication of wettability patterns and sculpturing complex 3D microstructures on the PEG basis. The swelling behavior of such morphological patterns was studied in detail, and it was shown that, in contrast to the pristine material, irradiated areas of the PEG films reveal an almost complete absence of the hydrogel-typical swelling behavior. The associated sealing of the irradiated areas allows a controlled deposition of objects dissolved in water, such as metal nanoparticles or fluorophores, into the surrounding, pristine areas, resulting in the formation of nanocomposite patterns. In contrast, due to the distinct protein-repelling properties of the PEG films, proteins are exclusively adsorbed onto the irradiated areas. This makes such films a suitable platform to prepare protein-affinity patterns in a protein-repelling background.

  16. High-pressure reactions in polyethylene films, a new development in matrix isolation. The photochemical reaction of Fe (CO) 5 with N 2 and the thermal reaction of Fe (CO) 4 (N 2) with H 2

    NASA Astrophysics Data System (ADS)

    Cooper, Andrew I.; Poliakoff, Martyn

    1993-09-01

    A new miniature high-pressure cell has been developed for the spectroscopic study of reactions between organometallic compounds impregnated into polymer films and gases such as N 2 or H 2 at any temperature between ambient and 20 K. The use of the cell is illustrated by the photochemical reactions of Fe(CO) 5 in polyethylene film (PE) with N 2 and H 2 at 190 K to form Fe (CO) 4(N 2) and Fe (CO) 4H 2 respectively. IR spectra suggest that the N 2 group may occupy an equatorial rather than an axial position. Once formed, Fe (CO) 4(N 2) is shown to react thermally with H 2 at ≈ 210 K to yield the dihydride compound, Fe (CO) 4H 2.

  17. Lithium-Salt-Containing High-Molecular-Weight Polystyrene-block-Polyethylene Oxide Block Copolymer Films.

    PubMed

    Metwalli, Ezzeldin; Rasool, Majid; Brunner, Simon; Müller-Buschbaum, Peter

    2015-08-10

    Ionic conductivity in relation to the morphology of lithium-doped high-molecular-weight polystyrene-block-polyethylene oxide (PS-b-PEO) diblock copolymer films was investigated as solid-state membranes for lithium-ion batteries. The tendency of the polyethylene (PEO) block to crystallize was highly suppressed by increasing both the salt-doping level and the temperature. The PEO crystallites completely vanished at a salt-doping ratio of Li/EO>0.08, at which the PEO segments were hindered from entering the crystalline unit of the PEO chain. A kinetically trapped lamella morphology of PS-b-PEO was observed, due to PEO crystallization. The increase in the lamella spacing with increasing salt concentration was attributed to the conformation of the PEO chain rather than the volume contribution of the salt or the previously reported increase in the effective interaction parameter. Upon loading the salt, the PEO chains changed from a compact/highly folded conformation to an amorphous/expanded-like conformation. The ionic conductivity was enhanced by amorphization of PEO and thereby the mobility of the PEO blocks increased upon increasing the salt-doping level.

  18. Application of schlieren interferometry to temperature measurements during laser welding of high-density polyethylene films.

    PubMed

    Coelho, João M P; Abreu, Manuel A; Rodrigues, F Carvalho

    2003-11-01

    Schlieren interferometry is found to be an alternative tool for temperature measurement during thermoplastic laser welding with regard to methods based on thermocouples or optical pyrometers. In fact, these techniques are not easily applied when materials to be processed have reduced thickness, negligible heat conduction, and low emissivity, as is the case of welding high-density polyethylene films with 10.6-microm CO2 laser radiation, even if the method reaches its applicability limit after approximately 1 s of the interaction process. The schlieren method provides the means and the results to probe the thermal variations of the laser-thermoplastic interaction on both the surface and the interface between the sample material and the air.

  19. Bendable ZnO thin film surface acoustic wave devices on polyethylene terephthalate substrate

    SciTech Connect

    He, Xingli; Guo, Hongwei; Chen, Jinkai; Wang, Wenbo; Xuan, Weipeng; Xu, Yang E-mail: jl2@bolton.ac.uk; Luo, Jikui E-mail: jl2@bolton.ac.uk

    2014-05-26

    Bendable surface acoustic wave (SAW) devices were fabricated using high quality c-axis orientation ZnO films deposited on flexible polyethylene terephthalate substrates at 120 °C. Dual resonance modes, namely, the zero order pseudo asymmetric (A{sub 0}) and symmetric (S{sub 0}) Lamb wave modes, have been obtained from the SAW devices. The SAW devices perform well even after repeated flexion up to 2500 με for 100 times, demonstrating its suitability for flexible electronics application. The SAW devices are also highly sensitive to compressive and tensile strains, exhibiting excellent anti-strain deterioration property, thus, they are particularly suitable for sensing large strains.

  20. Electron beam irradiation induced compatibilization of immiscible polyethylene/ethylene vinyl acetate (PE/EVA) blends: Mechanical properties and morphology stability

    NASA Astrophysics Data System (ADS)

    Entezam, Mehdi; Aghjeh, Mir Karim Razavi; Ghaffari, Mehdi

    2017-02-01

    Gel content, mechanical properties and morphology of immiscible PE/EVA blends irradiated by high energy electron beam were studied. The results of gel content measurements showed that the capability of cross-linking of the blend samples increased with an increase of the EVA composition. Also, the gel content for most compositions of the blends displayed a positive deviation from the additive rule. The results of mechanical properties showed that the tensile strength and elongation at break of the samples increased and decreased, respectively, with irradiation dose. On the other hand, the mechanical properties of the irradiated blends also depicted a positive deviation from additive rule contrary to the un-irradiated blends. A synergistic effect observed for the mechanical properties improvement of the irradiated blends and it was attributed to the probable formation of the PE-graft-EVA copolymers at the interface of the blends during the irradiation process. A theoretical analysis revealed that irradiation induced synergistic effect was more significant for EVA-rich blends with weaker interfacial interaction as compared to PE-rich blends. The morphological analysis indicated that the blend morphology was not affected obviously, whereas it was stabilized by irradiation.

  1. Intracellular calcium response and adhesiveness of chick embryonic retinal neurons to photoelectric dye-coupled polyethylene films as prototypes of retinal prostheses.

    PubMed

    Uji, Akihito; Matsuo, Toshihiko; Uchida, Tetsuya; Shimamura, Kaoru; Ohtsuki, Hiroshi

    2006-09-01

    Photoelectric dyes, which absorb light and convert photon energy to electric potentials, were shown to stimulate retinal neurons in culture. One of these dyes coupled with polyethylene film surface, as a prototype of retinal prostheses, could induce intracellular calcium elevation in chick embryonic retinal tissues. In this study, we used retinal cells from chick embryos in which no photoreceptor outer segments yet developed, and assessed cell adhesiveness and response to the original and modified types of our retinal prostheses. Extruded-blown film of high density polyethylene was used as the original polyethylene film. Polyethylene film surface was modified either by coupling with type 1 collagen or by crystallization from the melt of the original polyethylene film. A photoelectric dye, 2-[2-[4-(dibutylamino)phenyl]ethenyl]-3-carboxymethylbenzothiazolium bromide, was coupled to these different types of polyethylene films through amide linkage. Retinal cells from chick embryos at the 12-day embryonic stage were cultured on the surface of dye-coupled films. The response of retinal cells to the dye-coupled films was observed by calcium imaging. Cell types, either neurons or glial cells, were detected by immunocytochemical staining and also observed by scanning electron microscopy (SEM). Intracellular calcium elevation was observed in cells, including both neurons and glial cells, on the surface of the original dye-coupled film, collagen-coated dye-coupled film, and dye-coupled recrystallized film, in contrast with no response of cells cultured on the dye-uncoupled plain film. Retinal neurons grew upon colonies of glial cells settling on the surface of all different types of the films. The number of retinal neurons on the collagen-coated dye-coupled film and dye-coupled recrystallized film was significantly larger than the number of neurons on the dye-uncoupled plain film (P = 0.0004, analysis of variance; P < 0.05, Tukey-Kramer test). With SEM, Muller cell

  2. Environmentally Assisted Cracking in Silicon Nitride Barrier Films on Poly(ethylene terephthalate) Substrates.

    PubMed

    Kim, Kyungjin; Luo, Hao; Singh, Ankit K; Zhu, Ting; Graham, Samuel; Pierron, Olivier N

    2016-10-03

    A singular critical onset strain value has been used to characterize the strain limits of barrier films used in flexible electronics. However, such metrics do not account for time-dependent or environmentally assisted cracking, which can be critical in determining the overall reliability of these thin-film coatings. In this work, the time-dependent channel crack growth behavior of silicon nitride barrier films on poly(ethylene terephthalate) (PET) substrates is investigated in dry and humid environments by tensile tests with in situ optical microscopy and numerical models. The results reveal the occurrence of environmentally assisted crack growth at strains well below the critical onset crack strain and in the absence of polymer-relaxation-assisted, time-dependent crack growth. The crack growth rates in laboratory air are about 1 order of magnitude larger than those tested in dry environments (dry air or dry nitrogen). In laboratory air, crack growth rates increase from ∼200 nm/s to 60 μm/s for applied stress intensity factors, K, ranging from 1.0 to 1.4 MPa·m(1/2), below the measured fracture toughness Kc of 1.8 MPa·m(1/2). The crack growth rates in dry environments were also strongly dependent on the prior storage of the specimens, with larger rates for specimens exposed to laboratory air (and therefore moisture) prior to testing compared to specimens stored in a dry environment. This behavior is attributed to moisture-assisted cracking, with a measured power law exponent of ∼22 in laboratory air. This study also reveals that much larger densities of channel cracks develop in the humid environment, suggesting an easier initiation of channel cracks in the presence of water vapor. The results obtained in this work are critical to address the time-dependent and environmental reliability issues of thin brittle barriers on PET substrates for flexible electronics applications.

  3. Indium tin oxide films deposited by thermionic-enhanced DC magnetron sputtering on unheated polyethylene terephthalate polymer substrate

    SciTech Connect

    Lan, Y.F.; Peng, W.C.; Lo, Y.H.; He, J.L.

    2009-08-05

    Indium tin oxide thin films were deposited onto polyethylene terephthalate substrates via thermionic enhanced DC magnetron sputtering at low substrate temperatures. The structural, optical and electrical properties of these films are methodically investigated. The results show that compared with traditional sputtering, the films deposited with thermionic emission exhibit higher crystallinity, and their optical and electrical properties are also improved. Indium tin oxide films deposited by utilizing thermionic emission exhibit an average visible transmittance of 80% and an electrical resistivity of 4.5 x 10{sup -4} {Omega} cm, while films made without thermionic emission present an average visible transmittance of 74% and an electrical resistivity of 1.7 x 10{sup -3} {Omega} cm.

  4. Fe-Si-Cr/PTFE magnetic composite thick films on polyethylene terephthalate sheets for near field communications by aerosol deposition.

    PubMed

    Kim, Hyung-Jun; Nam, Song-Min; Koh, Jung-Hyuk

    2014-10-01

    Thick film growth of Fe-Si-Cr/poly-tetra-fluoro-ethylene (PTFE) composite films on polyethylene terephthalate (PET) sheets was investigated by aerosol deposition (AD) as a magnetic absorber for near field communication. The Fe-Si-Cr flakes were crushed to micro flakes smaller than 1 μm after the deposition, and formed dense microstructure on the PET sheets. The Fe-Si-Cr/PTFE composite thick films using 0.2 wt.% PTFE starting powder showed dense and uniform microstructure compared to the 0.5 wt.% film. The real relative permeability /' and the imaginary permeability μ" of Fe-Si-Cr/PTFE composite thick films using the 0.2 wt.% PTFE starting powder were 13.1 and 2.9 at 13.56 MHz, respectively. In the case of 0.5 wt.%, μ' and μ" respectively decreased to 7.4 and 1.0 at 13.56 MHz caused by adding PTFE.

  5. Effects of pre-annealing on the uni- and bi-axial stretching behavior of poly(ethylene naphthalate) films

    SciTech Connect

    Abe, T. Takarada, W. Kikutani, T.

    2014-05-15

    Effect of pre-annealing on stress and birefringence behavior of poly(ethylene naphthalate) (PEN) films during stretching and relaxation processes was investigated. Amorphous and non-oriented PEN films were pre-annealed under the conditions of different temperatures and periods. The pre-annealed films were stretched uniaxially or equi-biaxially and then relaxed at fixed length. It was found that pre-annealing did not cause any notable change for the initial behavior of refractive indices variation, whereas the behaviors after necking were significantly affected. Through the comparison between in-plane and out-of-plane birefringence and the analysis of wide-angle x-ray diffraction patterns of drawn films of both stretching modes, it was confirmed that the orientation of naphthalene ring in the film plane was enhanced by pre-annealing.

  6. Contamination characteristics and degradation behavior of low-density polyethylene film residues in typical farmland soils of China.

    PubMed

    Xu, Gang; Wang, Qunhui; Gu, Qingbao; Cao, Yunzhe; DU, Xiaoming; Li, Fasheng

    2006-01-01

    Low-density polyethylene (LDPE) film residues left in farmlands due to agricultural activities were extensively investigated to evaluate the present pollution situation by selecting the typical areas with LDPE film application, including Harbin, Baoding, and Handan of China. The survey results demonstrated that the film residues were ubiquitous within the investigated areas and the amount reached 2,400-8,200 g ha(-1). Breakage rates of the film residues were almost at the same level in the studied fields. There were relatively small amounts of film residues remaining in neighboring farmland fields without application of LDPE film. The studies showed that the sheets of LDPE residues had the same oxidative deterioration, which was probably due to photodegradation instead of biodegradation. The higher molecular weight components of the LDPE film gradually decreased, which were reflected by the appearance of some small flakes detached from the film bodies. LDPE films in the investigated fields gradually deteriorated and the decomposing levels developed with their left time increasing. The degradation behaviors of LDPE films were confirmed by using Fourier transform infrared (FTIR), scanning electron microscopic (SEM), and gel permeation chromatography analyses.

  7. Amperometric Biosensor Based on Zirconium Oxide/Polyethylene Glycol/Tyrosinase Composite Film for the Detection of Phenolic Compounds

    PubMed Central

    Ahmad, Nor Monica; Abdullah, Jaafar; Yusof, Nor Azah; Ab Rashid, Ahmad Hazri; Abd Rahman, Samsulida; Hasan, Md. Rakibul

    2016-01-01

    A phenolic biosensor based on a zirconium oxide/polyethylene glycol/tyrosinase composite film for the detection of phenolic compounds has been explored. The formation of the composite film was expected via electrostatic interaction between hexacetyltrimethylammonium bromide (CTAB), polyethylene glycol (PEG), and zirconium oxide nanoparticles casted on screen printed carbon electrode (SPCE). Herein, the electrode was treated by casting hexacetyltrimethylammonium bromide on SPCE to promote a positively charged surface. Later, zirconium oxide was mixed with polyethylene glycol and the mixture was dropped cast onto the positively charged SPCE/CTAB. Tyrosinase was further immobilized onto the modified SPCE. Characterization of the prepared nanocomposite film and the modified SPCE surface was investigated by scanning electron microscopy (SEM), Electrochemical Impedance Spectroscopy (EIS), and Cyclic voltamogram (CV). The developed biosensor exhibits rapid response for less than 10 s. Two linear calibration curves towards phenol in the concentrations ranges of 0.075–10 µM and 10–55 µM with the detection limit of 0.034 µM were obtained. The biosensor shows high sensitivity and good storage stability for at least 30 days. PMID:27367738

  8. Amperometric Biosensor Based on Zirconium Oxide/Polyethylene Glycol/Tyrosinase Composite Film for the Detection of Phenolic Compounds.

    PubMed

    Ahmad, Nor Monica; Abdullah, Jaafar; Yusof, Nor Azah; Ab Rashid, Ahmad Hazri; Abd Rahman, Samsulida; Hasan, Md Rakibul

    2016-06-29

    A phenolic biosensor based on a zirconium oxide/polyethylene glycol/tyrosinase composite film for the detection of phenolic compounds has been explored. The formation of the composite film was expected via electrostatic interaction between hexacetyltrimethylammonium bromide (CTAB), polyethylene glycol (PEG), and zirconium oxide nanoparticles casted on screen printed carbon electrode (SPCE). Herein, the electrode was treated by casting hexacetyltrimethylammonium bromide on SPCE to promote a positively charged surface. Later, zirconium oxide was mixed with polyethylene glycol and the mixture was dropped cast onto the positively charged SPCE/CTAB. Tyrosinase was further immobilized onto the modified SPCE. Characterization of the prepared nanocomposite film and the modified SPCE surface was investigated by scanning electron microscopy (SEM), Electrochemical Impedance Spectroscopy (EIS), and Cyclic voltamogram (CV). The developed biosensor exhibits rapid response for less than 10 s. Two linear calibration curves towards phenol in the concentrations ranges of 0.075-10 µM and 10-55 µM with the detection limit of 0.034 µM were obtained. The biosensor shows high sensitivity and good storage stability for at least 30 days.

  9. 21 CFR 172.260 - Oxidized polyethylene.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Oxidized polyethylene. 172.260 Section 172.260... CONSUMPTION Coatings, Films and Related Substances § 172.260 Oxidized polyethylene. Oxidized polyethylene may... polyethylene is the basic resin produced by the mild air oxidation of polyethylene. The polyethylene used...

  10. 21 CFR 172.260 - Oxidized polyethylene.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Oxidized polyethylene. 172.260 Section 172.260... CONSUMPTION Coatings, Films and Related Substances § 172.260 Oxidized polyethylene. Oxidized polyethylene may... polyethylene is the basic resin produced by the mild air oxidation of polyethylene. The polyethylene used...

  11. 21 CFR 172.260 - Oxidized polyethylene.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Oxidized polyethylene. 172.260 Section 172.260... CONSUMPTION Coatings, Films and Related Substances § 172.260 Oxidized polyethylene. Oxidized polyethylene may... polyethylene is the basic resin produced by the mild air oxidation of polyethylene. The polyethylene used...

  12. Enhanced electrochromic properties of TiO2 nanoporous film prepared based on an assistance of polyethylene glycol

    NASA Astrophysics Data System (ADS)

    Xu, Shunjian; Luo, Xiaorui; Xiao, Zonghu; Luo, Yongping; Zhong, Wei; Ou, Hui; Li, Yinshuai

    2017-01-01

    Polyethylene glycol (PEG) was employed as pore-forming agent to prepare TiO2 nanoporous film based on spin-coating a TiO2 nanoparticle mixed paste on fluorine doped tin oxide (FTO) glass. The electrochromic and optical properties of the obtained TiO2 film were investigated by cyclic voltammetry (CV), chronoamperometry (CA) and UV–Vis spectrophotometer. The results show that the PEG in the mixed paste endows the TiO2 film with well-developed porous structure and improves the uniformity of the TiO2 film, which are helpful for the rapid intercalation and extraction of lithium ions within the TiO2 film and the strengthening of the diffuse reflection of visible light in the TiO2 film. As a result, the TiO2 film derived from the mixed paste with PEG displays higher electrochemical activity and more excellent electrochromic performances compared with the TiO2 film derived from the mixed paste without PEG. The switching times of coloration/bleaching are respectively 10.16/5.65 and 12.77/6.13 s for the TiO2 films with PEG and without PEG. The maximum value of the optical contrast of the TiO2 film with PEG is 21.2% while that of the optical contrast of the TiO2 film without PEG is 14.9%. Furthermore, the TiO2 film with PEG has better stability of the colored state than the TiO2 film without PEG.

  13. A quartz crystal microbalance simulation to examine the effect of ultraviolet light treatment on characteristics of polyethylene surface.

    PubMed

    Gotoh, Keiko; Tagawa, Yumiko; Tabata, Izumi

    2008-01-01

    The effect of ultraviolet light irradiation on the characteristics of the polyethylene (PE) surface was investigated by the quartz crystal microbalance (QCM) technique. The PE film was prepared on the gold electrodes of the QCM by spin-coating from the solution and then was treated by the excimer UV lamp in ambient air. The changes in the hydrophilic properties, moisture adsorption, and water retention of the PE film due to the UV irradiation were determined from the frequency change of the QCM. To evaluate the detergency of the PE film, stearic acid as model oily soil was deposited onto the PE film formed on the QCM by the Langmuir-Blodgett (LB) technique, and was ultrasonically cleaned in aqueous detergent solutions containing ethanol or surfactant. The removal efficiency obtained from the frequency change of the QCM was found to increase considerably after the UV irradiation. From independently determined contact angles and the surface free energy components of the PE film, the free energy change resulting from the penetration of the detergent solution between stearic acid and PE in the zone of contact was calculated. Good relation was found between the removal efficiency and the free energy change, indicating that the increase in the detergency of the PE surface by UV irradiation was explained by surface energetics.

  14. Mechanical properties of polyurethane film exposed to solutions of nonoxynol-9 surfactant and polyethylene glycol

    NASA Astrophysics Data System (ADS)

    McDermott, Martin Kendrick

    Changes in physical properties (tensile strength, strain to failure, elastic modulus, diffusion kinetics and soft segment glass transition temperature (Tg)) were examined for polyetherurethane block copolymers Estane and Tecoflex. These polymer chains consist of 2 mutually incompatible blocks or segments which form microphases consisting of rigid/hard segments in an elastomeric matrix of soft segments. The polyurethanes were exposed to mixtures of nonoxynol 9 (N9) surfactant in polyethylene glycol 400 (PEG) at various concentrations and for various times. The purpose was to estimate the effect of exposure to mixtures of N9 spermicide and PEG lubricant on breakage of condoms made from films of these elastomers. Mechanical properties of Estane varied with direction because of molecular orientation induced during manufacturing, suggesting that condoms should be cut from the film in a way that optimizes this property-orientation relationship. Large amounts of N9 were absorbed from N9/PEG solutions. The polymer fraction of the swollen Estane film versus soak solution composition did not follow a linear rule of mixtures. As the percentage of N9 in the PEG/N9 soak solution increased, Estane absorbed more liquid and its properties decreased more than did Tecoflex. This may not matter for low concentrations of N9 where the mechanical properties of Estane were superior to those of Tecoflex. The loss of mechanical properties with increased N9 concentration was likely due to plasticization of the soft segment domains. Hard segment domain disruption was probably not occurring because the relationship between the elastic modulus and polymer volume fraction followed the Flory-Rehner relationship for swollen elastic rubber networks and diffusion of neat N9 and neat PEG followed a Fickian behavior. This is expected because hard domains are much more difficult to disrupt due to strong hydrogen bonding and/or crystallization. Most of the absorption and decrease in mechanical

  15. Biofilm and Diatom Succession on Polyethylene (PE) and Biodegradable Plastic Bags in Two Marine Habitats: Early Signs of Degradation in the Pelagic and Benthic Zone?

    PubMed

    Eich, Andreas; Mildenberger, Tobias; Laforsch, Christian; Weber, Miriam

    2015-01-01

    The production of biodegradable plastic is increasing. Given the augmented littering of these products an increasing input into the sea is expected. Previous laboratory experiments have shown that degradation of plastic starts within days to weeks. Little is known about the early composition and activity of biofilms found on biodegradable and conventional plastic debris and its correlation to degradation in the marine environment. In this study we investigated the early formation of biofilms on plastic shopper bags and its consequences for the degradation of plastic. Samples of polyethylene and biodegradable plastic were tested in the Mediterranean Sea for 15 and 33 days. The samples were distributed equally to a shallow benthic (sedimentary seafloor at 6 m water depth) and a pelagic habitat (3 m water depth) to compare the impact of these different environments on fouling and degradation. The amount of biofilm increased on both plastic types and in both habitats. The diatom abundance and diversity differed significantly between the habitats and the plastic types. Diatoms were more abundant on samples from the pelagic zone. We anticipate that specific surface properties of the polymer types induced different biofilm communities on both plastic types. Additionally, different environmental conditions between the benthic and pelagic experimental site such as light intensity and shear forces may have influenced unequal colonisation between these habitats. The oxygen production rate was negative for all samples, indicating that the initial biofilm on marine plastic litter consumes oxygen, regardless of the plastic type or if exposed in the pelagic or the benthic zone. Mechanical tests did not reveal degradation within one month of exposure. However, scanning electron microscopy (SEM) analysis displayed potential signs of degradation on the plastic surface, which differed between both plastic types. This study indicates that the early biofilm formation and composition

  16. Biofilm and Diatom Succession on Polyethylene (PE) and Biodegradable Plastic Bags in Two Marine Habitats: Early Signs of Degradation in the Pelagic and Benthic Zone?

    PubMed Central

    Laforsch, Christian; Weber, Miriam

    2015-01-01

    The production of biodegradable plastic is increasing. Given the augmented littering of these products an increasing input into the sea is expected. Previous laboratory experiments have shown that degradation of plastic starts within days to weeks. Little is known about the early composition and activity of biofilms found on biodegradable and conventional plastic debris and its correlation to degradation in the marine environment. In this study we investigated the early formation of biofilms on plastic shopper bags and its consequences for the degradation of plastic. Samples of polyethylene and biodegradable plastic were tested in the Mediterranean Sea for 15 and 33 days. The samples were distributed equally to a shallow benthic (sedimentary seafloor at 6 m water depth) and a pelagic habitat (3 m water depth) to compare the impact of these different environments on fouling and degradation. The amount of biofilm increased on both plastic types and in both habitats. The diatom abundance and diversity differed significantly between the habitats and the plastic types. Diatoms were more abundant on samples from the pelagic zone. We anticipate that specific surface properties of the polymer types induced different biofilm communities on both plastic types. Additionally, different environmental conditions between the benthic and pelagic experimental site such as light intensity and shear forces may have influenced unequal colonisation between these habitats. The oxygen production rate was negative for all samples, indicating that the initial biofilm on marine plastic litter consumes oxygen, regardless of the plastic type or if exposed in the pelagic or the benthic zone. Mechanical tests did not reveal degradation within one month of exposure. However, scanning electron microscopy (SEM) analysis displayed potential signs of degradation on the plastic surface, which differed between both plastic types. This study indicates that the early biofilm formation and composition

  17. Control of carbon content in amorphous GeTe films deposited by plasma enhanced chemical vapor deposition (PE-MOCVD) for phase-change random access memory applications

    NASA Astrophysics Data System (ADS)

    Aoukar, M.; Szkutnik, P. D.; Jourde, D.; Pelissier, B.; Michallon, P.; Noé, P.; Vallée, C.

    2015-07-01

    Amorphous and smooth GeTe thin films are deposited on 200 mm silicon substrates by plasma enhanced—metal organic chemical vapor deposition (PE-MOCVD) using the commercial organometallic precursors TDMAGe and DIPTe as Ge and Te precursors, respectively. X-ray photoelectron spectroscopy (XPS) measurements show a stoichiometric composition of the deposited GeTe films but with high carbon contamination. Using information collected by Optical Emission Spectroscopy (OES) and XPS, the origin of carbon contamination is determined and the dissociation mechanisms of Ge and Te precursors in H2 + Ar plasma are proposed. As a result, carbon level is properly controlled by varying operating parameters such as plasma radio frequency power, pressure and H2 rate. Finally, GeTe films with carbon level as low as 5 at. % are obtained.

  18. Effect of antioxidants and light stabilisers on silver migration from nanosilver-polyethylene composite packaging films into food simulants.

    PubMed

    Su, Qi-Zhi; Lin, Qin-Bao; Chen, Chao-Fang; Wu, Yu-Mei; Wu, Li-Bing; Chen, Xiao-Qing; Wang, Zhi-Wei

    2015-01-01

    The effect of exposure time, temperature and food simulants, especially additives, on the release of silver from nanosilver-polyethylene composite films to food simulants was studied. Two different type of nanosilver-polyethylene composite films (with or without additives) were chosen to conduct the experiment with the aim of exploring the behaviour of silver migration. It was shown that the migration of silver into 50% ethanol at 40 and 70°C was much less than that into 3% acetic acid. With the increase of exposure time and temperature, the release of silver increased. The migration even continued after a long exposure time (14 days at 20°C, 10 days at 40°C, and 6 days at 70°C respectively). Only about 0.15‰ of silver migrated from composite films with the additives into 3% acetic acid after 6 days of exposure at 70°C, while about 1.3% of silver migrated from composite films that did not contain additives under the same conditions. This could be because the addition of the antioxidants and light stabilisers prevents silver from being oxidised, which is an important way for the release of silver.

  19. Low-temperature atomic layer deposition of Al{sub 2}O{sub 3} on blown polyethylene films with plasma-treated surfaces

    SciTech Connect

    Beom Lee, Gyeong; Sik Son, Kyung; Won Park, Suk; Hyung Shim, Joon; Choi, Byoung-Ho

    2013-01-15

    In this study, a layer of Al{sub 2}O{sub 3} was deposited on blown polyethylene films by atomic layer deposition (ALD) at low temperatures, and the surface characteristics of these Al{sub 2}O{sub 3}-coated blown polyethylene films were analyzed. In order to examine the effects of the plasma treatment of the surfaces of the blown polyethylene films on the properties of the films, both untreated and plasma-treated film samples were prepared under various processing conditions. The surface characteristics of the samples were determined by x-ray photoelectron spectroscopy, as well as by measuring their surface contact angles. It was confirmed that the surfaces of the plasma-treated samples contained a hydroxyl group, which helped the precursor and the polyethylene substrate to bind. ALD of Al{sub 2}O{sub 3} was performed through sequential exposures to trimethylaluminum and H{sub 2}O at 60 Degree-Sign C. The surface morphologies of the Al{sub 2}O{sub 3}-coated blown polyethylene films were observed using atomic force microscopy and scanning electron microscopy/energy-dispersive x-ray spectroscopy. Further, it was confirmed that after ALD, the surface of the plasma-treated film was covered with alumina grains more uniformly than was the case for the surface of the untreated polymer film. It was also confirmed via the focused ion beam technique that the layer Al{sub 2}O{sub 3} conformed to the surface of the blown polyethylene film.

  20. Solution and film properties of sodium caseinate/glycerol and sodium caseinate/polyethylene glycol edible coating systems.

    PubMed

    Siew, D C; Heilmann, C; Easteal, A J; Cooney, R P

    1999-08-01

    The aim of this study is to determine the effects of plasticizer hydrogen bonding capability and chain length on the molecular structure of sodium caseinate (NaCAS), in NaCAS/glycerol and NaCAS/polyethylene glycol 400 (PEG) systems. Both solution and film phases were investigated. Glycerol and PEG reduced the viscosity of aqueous NaCAS, with the latter having a greater effect. This was explained in terms of protein/plasticizer aggregate size and changes to the conformation of the caseinate chain. In the film phase, glycerol caused more pronounced changes to the film tensile strength compared with PEG. However, the effect of glycerol on film water vapor permeability was smaller. These observations are attributed to the differences in plasticizer size and hydrogen bonding strength that controls the protein-plasticizer and protein-protein interactions in the films. Glass transition calculations from the tensile strength data indicate that the distribution of bonding interactions is more homogeneous in NaCAS/PEG films than in NaCAS/glycerol films.

  1. Room temperature crystallization of indium tin oxide films on glass and polyethylene terephthalate substrates using rf plasma

    SciTech Connect

    Ohsaki, H.; Suzuki, M.; Shibayama, Y.; Kinbara, A.; Watanabe, T.

    2007-07-15

    The crystallization of amorphous indium tin oxide (ITO) films was achieved by rf (13.56 MHz) plasma treatment. Although the films were crystallized after 2 min, the sample temperature was lower than 90 deg. C without compulsory cooling even after 10 min of treatment and polyethylene terephthalate (PET) substrates had no damage. Plasma-crystallized sputtered ITO films have a bixbite structure and the resistivity reached to 1.6x10{sup -4} {omega}{center_dot}cm. ITO thin films have almost the same resistivity in both cases of PET and glass substrates used and plasma-treated PET ITO films have a bit higher resistivity than that of glass ITO films, while mass spectroscopy measurements indicated that ITO films deposited on PET substrates are expected to include no apparent gas species ejected from PET substrate. It was found that the plasma gas pressure is the key parameter for the effective crystallization and the appropriate gas pressure depends on the plasma gas species.

  2. Polyethylene Films Containing Silver Nanoparticles for Applications in Food Packaging: Characterization of Physico-Chemical and Anti-Microbial Properties.

    PubMed

    Becaro, Aline A; Puti, Fernanda C; Correa, Daniel S; Paris, Elaine C; Marconcini, José M; Ferreira, Marcos D

    2015-03-01

    This paper reports the antibacterial effect and physico-chemical characterization of films containing silver nanoparticles for use as food packaging. Two masterbatches (named PEN and PEC) con- taining silver nanoparticles embedded in distinct carriers (silica and titanium dioxide) were mixed with low-density polyethylene (LDPE) in different compositions and extruded to produce plain films. These films were characterized by Scanning Electron Microscopy (SEM), X-ray diffraction (XRD), Differential Scanning Calorimetry (DSC), Thermogravimetric analysis (TGA) and Fourier Transform Infrared Spectroscopy (FTIR). The morphology of the films showed the formation of agglomerates of nanoparticles in both PEN and PEC composites. X-ray analyses confirmed the presence of SiO2 in PEN samples and TiO2 in PEC samples. Thermal analyses indicated an increase in thermal stability of the PEC compositions. The antimicrobial efficacy was determined by applying the test strain for Escherichia coli and Staphylococcus aureus, according to the Japanese Industrial Standard Method (JIS Z 2801:2000). The films analyzed showed antimicrobial properties against the tested microorganisms, presenting better activity against the S. aureus than E. Coli. These findings suggest that LDPE films with silver nanoparticles are promising to provide a significant contribution to the quality and safety of packaged food.

  3. Plasma treated polyethylene terephthalate/polypropylene films assembled with chitosan and various preservatives for antimicrobial food packaging.

    PubMed

    Lei, Jieqiong; Yang, Lingxiao; Zhan, Yingfei; Wang, Yuntao; Ye, Ting; Li, Yan; Deng, Hongbing; Li, Bin

    2014-02-01

    In this study, polyethylene terephthalate/polypropylene (PET/PP) films were treated via atmospheric pressure plasma, assembled with chitosan and various preservatives and applied for antimicrobial food packaging. Surface properties of these obtained films were studied by contact angle measurement, atomic force microscopy (ATM), X-ray photoelectron spectroscopy (XPS), Fourier transformed infrared spectroscopy (FT-IR) and dynamic laser scattering (DLS). The above results showed that the surface hydrophilicity and roughness of the films increased after the plasma treatment. Besides, chitosan and the preservatives were successfully assembled onto the surface of the films. In addition, the antimicrobial activities of the films against three kinds of microorganisms (Staphylococcus aureus, Bacillus subtilis and Escherichia coli) were investigated and the results indicated that the inhibition ratios against B. subtilis and E. coli reached almost 100% while the inhibition ratios against S. aureus were lower than 85%. Moreover, the accumulative release profiles of the antimicrobial substances migrating from the assembled films into the release solutions revealed that their release speed increased with the increment of temperature and acidity, but decreased with enhancing the ionic strength regulated by sodium chloride or with lowering the ionic mobility regulated by sucrose.

  4. Effect of molecular weight and concentration of polyethylene glycol on physicochemical properties and stability of shellac film.

    PubMed

    Luangtana-anan, Manee; Nunthanid, Jurairat; Limmatvapirat, Sontaya

    2010-12-22

    The effects of molecular weight and concentration of plasticizer on physicochemical properties and stability of shellac films were investigated. Type of plasticizer was previously reported to have some effects on the stability of shellac films, and polyethylene glycol (PEG) was the plasticizer of choice for plasticizing shellac films. In this study, different molecular weights of PEG (200, 400 and 4000) were chosen at a concentration of 10% w/w of shellac films. Shellac in alcohol was prepared in a free film. The stability of shellac film was then performed at 75% RH, 40 °C for 3 months. The comparison was made between the film with and without plasticizer. Shellac films were then determined for acid value, insoluble solid, mechanical properties and water vapor permeability coefficient. It was reported that different molecular weights of PEG had some influence on physicochemical properties of the shellac films. Among different molecular weights of PEG, PEG 400 showed a suitable molecular weight that could protect the shellac chain at the carboxylic and hydroxyl groups. Therefore, the molecular weight of plasticizer played a crucial role for the protective ability at active sites. Further study was performed to investigate the effect of concentrations of PEG 400 on the stability. The results demonstrated that PEG 400 at a concentration of 10% (w/w) could prevent the polymerization process for only 4 months and a significant change of all parameters was then reported. However, a higher concentration, 20% (w/w) of PEG 400, could prolong the stability of shellac for 6 months of study. Therefore, the drawback of shellac as a natural polymer in pharmaceutical and food industries could be tackled by the appropriate size and concentration of plasticizer.

  5. Polyethylene glycol-assisted growth of Cu2SnS3 promising absorbers for thin film solar cell applications

    NASA Astrophysics Data System (ADS)

    Kahraman, S.; Çetinkaya, S.; Yaşar, S.; Bilican, İ.

    2014-09-01

    In this paper, we report, for the first time, the results of the polyethylene glycol- (PEG) assisted preparation and characterization of high-quality and well-crystallized Cu2SnS3 (CTS) thin films obtained using sol-gel spin-coating method and a subsequent annealing in a sulphur atmosphere. Structural, morphological, compositional, electrical and optical investigations were carried out. The X-ray diffraction patterns of the samples proved the polycrystalline nature and preferred crystallization of the films. No peak referring to other binary or ternary phases were detected in the patterns. The intensity of the preferred orientation and crystallite size of the films increased with increasing PEG content. This trend yielded an improvement in photo-transient currents of the PEG-assisted growth of CTS films. The scanning electron microscopy images revealed that the CTS films have continuous, dense and agglomeration-like morphology. Through energy dispersive X-ray spectroscopy studies, it has been deduced that the samples consist of Cu, Sn and S of which atomic percentages were consistent with Cu/Sn and S/metal initial ratios. The agglomerated morphology of the samples has been attributed to increasing PEG content. A remarkable enhancement was observed in photo-transient currents of p-n junction of the produced films along with increasing PEG content. Through resistivity-temperature measurements, three impurity level electrical activation energy values for each film were found. Optical band gap values of the films were estimated via absorbance-wavelength behaviours and decreased with increasing PEG content. It has been revealed that PEG-assisted growth of CTS thin films is a promising way to improve its photovoltaic characteristics.

  6. Aerobic deterioration stimulates outgrowth of spore-forming Paenibacillus in corn silage stored under oxygen-barrier or polyethylene films.

    PubMed

    Borreani, Giorgio; Dolci, Paola; Tabacco, Ernesto; Cocolin, Luca

    2013-08-01

    The occurrence of Bacillus and Paenibacillus spores in silage is of great concern to dairy producers because their spores can survive pasteurization and some strains are capable of subsequently germinating and growing under refrigerated conditions in pasteurized milk. The objectives of this study were to verify the role of aerobic deterioration of corn silage on the proliferation of Paenibacillus spores and to evaluate the efficacy of oxygen-barrier films used to cover silage during fermentation and storage to mitigate these undesirable bacterial outbreaks. The trial was carried out on whole-crop maize (Zea mays L.) inoculated with a mixture of Lactobacillus buchneri, Lactobacillus plantarum, and Enterococcus faecium. A standard polyethylene film and a polyethylene-polyamide film with an enhanced oxygen barrier were used to produce the silage bags for this experiment. The silos were stored indoors at ambient temperature (18 to 22°C) and opened after 110 d. The silage was sampled after 0, 2, 5, 7, 9, and 14 d of aerobic exposure to quantify the growth of endospore-forming bacteria during the exposure of silages to air. Paenibacillus macerans (gram-positive, facultatively anaerobic bacteria) was able to develop during the aerobic exposure of corn silage. This species was present in the herbage at harvesting, together with clostridial spores, and survived ensiling fermentation; it constituted more than 60% of the anaerobic spore formers at silage opening. During silage spoilage, the spore concentration of P. macerans increased to values greater than 7.0 log10 cfu/g of silage. The use of different plastic films to seal silages affected the growth of P. macerans and the number of spores during aerobic exposure of silages. These results indicate that the number of Paenibacillus spores could greatly increase in silage after exposure to air, and that oxygen-barrier films could help to reduce the potential for silage contamination of this important group of milk spoilage

  7. Usefulness of an aluminized polyester film for reducing heat in polyethylene calf hutches.

    PubMed

    Binion, W R; Friend, T H; Holub, G A

    2014-11-01

    This study determined the efficacy of a radiant barrier material used in the construction industry to moderate summer temperatures in polyethylene calf hutches. The cover consisted of a single layer of two-sided reflective aluminized polyester film with a center polyester scrim reinforcement (reflectivity = 95%). At each of two dairies, six hutches containing a young calf were either uncovered (control) or had reflective covers across the top and sides of the hutch, leaving the front, back, and 1.2 × 1.8-m attached outdoor wire pen exposed. Duplicate loggers mounted 20 cm above the flooring in the center of each hutch recorded interior temperature at 30-min intervals over 22 days during late August to early September. The mean daily interior peak temperatures in each of the hutches over 21 days of observation were significantly less (P < 0.001) in the hutches with reflective covers (37.48 ± 0.14 °C) than in the uncovered hutches (41.65 ± 0.45 °C) and did not differ (P = 0.77) between dairies. The mean daily interior peak temperatures in each of the hutches over the warmest 10 days of observation were significantly less (P < 0.001) in hutches with reflective covers (40.15 °C ± 0.16) than in the uncovered hutches (44.93 ± 0.47 °C). The mean interior ceiling temperatures in each of the hutches over 4 days of observation were significantly lower (P < 0.001) in the hutches with reflective covers (37.82 ± 0.36 °C) than in the uncovered hutches (46.89 ± 0.47 °C). The reflective cover used in this study moderated interior hutch temperatures but showed signs of delamination after 22 days and was relatively expensive, so more suitable material needs to be identified.

  8. The influence of guaifenesin and ketoprofen on the properties of hot-melt extruded polyethylene oxide films.

    PubMed

    Crowley, Michael M; Fredersdorf, Anke; Schroeder, Britta; Kucera, Shawn; Prodduturi, Suneela; Repka, Michael A; McGinity, James W

    2004-08-01

    Films containing polyethylene oxide (PEO) and a model drug, either guaifenesin (GFN) or ketoprofen (KTP), were prepared by hot-melt extrusion. The thermal properties of the hot-melt extruded films were investigated using differential scanning calorimetry (DSC). Scanning electron microscopy (SEM) was used to examine the surface morphology of the films, and wide angle X-ray diffraction (XRD) was used to investigate the crystalline properties of the polymer, drugs and physical mixtures as well as the solid state structure of the films. The stability of the polymer was studied using gel permeation chromatography. The mechanical properties, including percent elongation and tensile strength of the films, were determined on an Instron according to American Society for Testing Materials (ASTM) procedures. The Hansen solubility parameter was calculated using the Hoftyzer or van Krevelen method to estimate the likelihood of drug--polymer miscibility. Both GFN and KTP were stable during the extrusion process. Melting points corresponding to the crystalline drugs were not observed in the films. Crystallization of GFN on the surface of the film was observed at all concentrations studied, however KTP crystallization did not occur until reaching the 15% level. Guaifenesin and ketoprofen were found to decrease drive load, increase PEO stability and plasticize the polymer during extrusion. The Hansen solubility parameters predicted miscibility between PEO and KTP and poor miscibility between PEO and GFN. The predictions of the solubility parameters were in agreement with the XRD and SEM results. The percent elongation decreased with increasing GFN concentrations and significantly increased with increasing levels of KTP. Both GFN and KTP decreased the tensile strength of the extruded film.

  9. Nanoscale mechanical and tribological properties of fluorocarbon films grafted onto plasma-treated low-density polyethylene surfaces

    NASA Astrophysics Data System (ADS)

    Cheng, Q.; Komvopoulos, K.

    2012-03-01

    Fluorocarbon (FC) films were grafted onto Ar plasma-treated low-density polyethylene (LDPE) surfaces by plasma polymerization and deposition. The evolution of the surface morphology of the grafted FC films was investigated at different scales with an atomic force microscope. Nanoscale sliding experiments performed with a surface force microscope provided insight into the nanotribological properties of Ar plasma-treated LDPE, with and without grafted FC films, in terms of applied normal load and number of sliding cycles. The observed trends are explained in the context of microstructure models accounting for morphological and structure changes at the LDPE surface due to the effects of plasma treatment (e.g., selective etching of amorphous phase, chain crosslinking and FC film grafting) and surface sliding (e.g., crystalline lamellae alignment along the sliding direction). Nanoindentation experiments elucidated the effect of plasma treatment on surface viscoelasticity and global contact stiffness. The results of this study demonstrate that plasma-assisted grafting of FC films is an effective surface modification method for tuning the nanomechanical/tribological properties of polymers.

  10. Stepwise crystallization and the layered distribution in crystallization kinetics of ultra-thin poly(ethylene terephthalate) film

    NASA Astrophysics Data System (ADS)

    Zuo, Biao; Xu, Jianquan; Sun, Shuzheng; Liu, Yue; Yang, Juping; Zhang, Li; Wang, Xinping

    2016-06-01

    Crystallization is an important property of polymeric materials. In conventional viewpoint, the transformation of disordered chains into crystals is usually a spatially homogeneous process (i.e., it occurs simultaneously throughout the sample), that is, the crystallization rate at each local position within the sample is almost the same. Here, we show that crystallization of ultra-thin poly(ethylene terephthalate) (PET) films can occur in the heterogeneous way, exhibiting a stepwise crystallization process. We found that the layered distribution of glass transition dynamics of thin film modifies the corresponding crystallization behavior, giving rise to the layered distribution of the crystallization kinetics of PET films, with an 11-nm-thick surface layer having faster crystallization rate and the underlying layer showing bulk-like behavior. The layered distribution in crystallization kinetics results in a particular stepwise crystallization behavior during heating the sample, with the two cold-crystallization temperatures separated by up to 20 K. Meanwhile, interfacial interaction is crucial for the occurrence of the heterogeneous crystallization, as the thin film crystallizes simultaneously if the interfacial interaction is relatively strong. We anticipate that this mechanism of stepwise crystallization of thin polymeric films will allow new insight into the chain organization in confined environments and permit independent manipulation of localized properties of nanomaterials.

  11. Water effect on the surface morphology of TiO2 thin film modified by polyethylene glycol

    NASA Astrophysics Data System (ADS)

    Wang, Sheng-Hung; Wang, Kuo-Hua; Dai, Yong-Ming; Jehng, Jih-Mirn

    2013-01-01

    Water effect on the surface morphology of TiO2 thin film was investigated by using PEG-6000 as a template to form the porous structure. The porous TiO2 thin films were characterized by thermo-gravimetric analysis (TGA), X-ray diffraction (XRD), n&k Analyzer, UV-vis spectrophotometer, field-emission scanning electron microscopy (FE-SEM), and atomic forced microscopy (AFM) as a function of water content in the preparation of TiO2 thin film. The various water contents result in the TiO2 thin films possessing different surface structures, grain sizes, and thicknesses. The grain sizes were varied with changing the water content, and the thickness increased with increasing water content due to the enhancement of the cross-linking speed. In addition, the cratered surface structure transformed into cracked surface structure upon the water content beyond stoichiometric quantity because the excess water causes the aggregation of polyethylene glycol (PEG-6000). The photocatalysis has been performed by the degradation of methyl blue with corresponding structural characteristics of the TiO2 thin film. The best photocatalytic activity has been obtained when the ratio of water to titanium precursor is equal to 2 referred as TiO2-W2.

  12. Synthesis of polycarbonate-r-polyethylene glycol copolymer for templated synthesis of mesoporous TiO2 films.

    PubMed

    Patel, Rajkumar; Kim, Jinkyu; Lee, Chang Soo; Kim, Jong Hak

    2014-12-01

    We synthesized a novel polycarbonate Z-r-polyethylene glycol (PCZ-r-PEG) copolymer by solution polycondensation. Successful synthesis of PCZ-r-PEG copolymer was confirmed by Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance (1H-NMR), gel permeation chromatography (GPC), and transmission electron microscopy (TEM). PCZ-r-PEG copolymer was used as a structure-directing agent for fabrication of mesoporous thin film containing a titanium dioxide (TiO2) layer. To control the porosity of the resultant inorganic layer, the ratio of titanium(IV) isopropoxide (TTIP) to PCZ-r-PEG copolymer was varied. The structure and porosity of the resulting mesoporous films were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM) analyses. Mesoporous TiO2 films fabricated on an F-doped tin oxide (FTO) surface were used as photoanodes for quasi-solid-state dye-sensitized solar cells (qssDSSCs). The highest efficiency achieved was 3.3% at 100 mW/cm2 for a film thickness of 750 nm, which is high considering the thickness of TiO2 film, indicating the importance of the structure-directing agent.

  13. Plasma-Enhanced Chemical Vapor Deposition (PE-CVD) yields better Hydrolytical Stability of Biocompatible SiOx Thin Films on Implant Alumina Ceramics compared to Rapid Thermal Evaporation Physical Vapor Deposition (PVD).

    PubMed

    Böke, Frederik; Giner, Ignacio; Keller, Adrian; Grundmeier, Guido; Fischer, Horst

    2016-07-20

    Densely sintered aluminum oxide (α-Al2O3) is chemically and biologically inert. To improve the interaction with biomolecules and cells, its surface has to be modified prior to use in biomedical applications. In this study, we compared two deposition techniques for adhesion promoting SiOx films to facilitate the coupling of stable organosilane monolayers on monolithic α-alumina; physical vapor deposition (PVD) by thermal evaporation and plasma enhanced chemical vapor deposition (PE-CVD). We also investigated the influence of etching on the formation of silanol surface groups using hydrogen peroxide and sulfuric acid solutions. The film characteristics, that is, surface morphology and surface chemistry, as well as the film stability and its adhesion properties under accelerated aging conditions were characterized by means of X-ray photoelectron spectroscopy (XPS), energy dispersive X-ray spectroscopy (EDX), scanning electron microscopy (SEM), inductively coupled plasma-optical emission spectroscopy (ICP-OES), and tensile strength tests. Differences in surface functionalization were investigated via two model organosilanes as well as the cell-cytotoxicity and viability on murine fibroblasts and human mesenchymal stromal cells (hMSC). We found that both SiOx interfaces did not affect the cell viability of both cell types. No significant differences between both films with regard to their interfacial tensile strength were detected, although failure mode analyses revealed a higher interfacial stability of the PE-CVD films compared to the PVD films. Twenty-eight day exposure to simulated body fluid (SBF) at 37 °C revealed a partial delamination of the thermally deposited PVD films whereas the PE-CVD films stayed largely intact. SiOx layers deposited by both PVD and PE-CVD may thus serve as viable adhesion-promoters for subsequent organosilane coupling agent binding to α-alumina. However, PE-CVD appears to be favorable for long-term direct film exposure to aqueous

  14. Synthesis and Characterization of In2S3 Thin Films Deposited by Chemical Bath Deposition on Polyethylene Naphthalate Substrates

    NASA Astrophysics Data System (ADS)

    Castelo-González, O. A.; Santacruz-Ortega, H. C.; Quevedo-López, M. A.; Sotelo-Lerma, M.

    2012-04-01

    Indium sulfide (In2S3) thin films were deposited on polyethylene naphthalate (PEN) by chemical bath deposition (CBD). The materials were characterized by ultraviolet (UV)-visible spectroscopy, x-ray photoelectron spectroscopy (XPS), energy-dispersive x-ray spectroscopy (EDX), scanning electron microscopy (SEM), and x-ray diffraction (XRD) to investigate the influence of the polymeric substrate on the resulting thin In2S3. The films showed polycrystalline (cubic and tetragonal) structure. A reduction of the ordering of the polymeric chains at the surface of the PEN was also observed, demonstrated by the appearance of two infrared bands at 1094 cm-1 and 1266 cm-1. Presence of oxygen during the early stages of In2S3 growth was also identified. We propose a reaction mechanism for both the equilibrium and nucleation stages. These results demonstrate that In2S3 can be deposited at room temperature on a flexible substrate.

  15. Optical properties and infrared optics applications of composite films based on polyethylene and low-melting-point chalcogenide glass

    NASA Astrophysics Data System (ADS)

    Bormashenko, Edward; Pogreb, Roman; Sutovski, Semion; Levin, Mark

    2002-02-01

    A novel composite material based on medium-density polyethylene and thermoplastic chalcogenide glass has been produced. Both materials are highly transparent in the middle and far IR, but their refractive indices differ dramatically. The polymer and the glass have nearly equal viscosities at the temperature of polyethylene processing. This fact allowed the use of extrusion for homogenization. Single- and twin-screw extrusion processes yielded compositions that contain up to 40% of chalcogenide glass particles, which were dispersed in the polymer matrix. Highly homogeneous compositions that contain perfectly spherical glass particles 1 to 2 micrometers in diameter dispersed in the polymer matrix were obtained. Highly oriented structures involving chalcogenide glass fibers immersed in the polymer matrix were prepared at high stretch speeds. It was established that it is possible to produce a composite that is opaque in the visible and near IR, and highly transparent in the 2 to 25-micrometers wavelength band. The use of oriented films as IR laser light-shaping diffusers is possible. The composite films obtained were tried successfully as immersion adhesive layers for the contacting of IR fibers.

  16. Resistance to moist conditions of whey protein isolate and pea starch biodegradable films and low density polyethylene nondegradable films: a comparative study

    NASA Astrophysics Data System (ADS)

    Mehyar, G. F.; Bawab, A. Al

    2015-10-01

    Biodegradable packaging materials are degraded under the natural environmental conditions. Therefore using them could alleviate the problem of plastics accumulation in nature. For effective replacement of plastics, with biodegradable materials, biodegradable packages should keep their properties under the high relative humidity (RH) conditions. Therefore the objectives of the study were to develop biodegradable packaging material based on whey protein isolate (WPI) and pea starch (PS). To study their mechanical, oxygen barrier and solubility properties under different RHs compared with those of low density polyethylene (LDPE), the most used plastic in packaging. Films of WPI and PS were prepared separately and conditioned at different RH (30-90%) then their properties were studied. At low RHs (<50%), WPI films had 2-3 times lower elongation at break (E or stretchability) than PS and LDPE. Increasing RH to 90% significantly (P<0.01) increased the elongation of PS but not WPI and LDPE films. LDPE and WPI films kept significantly (P<0.01) higher tensile strength (TS) than PS films at high RH (90%). Oxygen permeability (OP) of all films was very low (<0.5 cm3 μm m-2 d-1 kPa-1) below 40% RH but increased for PS films and became significantly (P<0.01) different than that of LDPE and WPI at > 40% RH. Oxygen permeability of WPI and LDPE did not adversely affected by increasing RH to 65%. Furthermore, WPI and LDPE films had lower degree of hydration at 50% and 90% RH and total soluble matter than PS films. These results suggest that WPI could be successfully replacing LDPE in packaging of moist products.

  17. Facile modulation of cell adhesion to a poly(ethylene glycol) diacrylate film with incorporation of polystyrene nano-spheres.

    PubMed

    Yang, Wenguang; Yu, Haibo; Li, Gongxin; Wang, Yuechao; Liu, Lianqing

    2016-12-01

    Poly(ethylene glycol) diacrylate (PEGDA) is a common hydrogel that has been actively investigated for various tissue engineering applications owing to its biocompatibility and excellent mechanical properties. However, the native PEGDA films are known for their bio-inertness which can hinder cell adhesion, thereby limiting their applications in tissue engineering and biomedicine. Recently, nano composite technology has become a particularly hot topic, and has led to the development of new methods for delivering desired properties to nanomaterials. In this study, we added polystyrene nano-spheres (PS) into a PEGDA solution to synthesize a nano-composite film and evaluated its characteristics. The experimental results showed that addition of the nanospheres to the PEGDA film not only resulted in modification of the mechanical properties and surface morphology but further improved the adhesion of cells on the film. The tensile modulus showed clear dependence on the addition of PS, which enhanced the mechanical properties of the PEGDA-PS film. We attribute the high stiffness of the hybrid hydrogel to the formation of additional cross-links between polymeric chains and the nano-sphere surface in the network. The effect of PS on cell adhesion and proliferation was evaluated in L929 mouse fibroblast cells that were seeded on the surface of various PEGDA-PS films. Cells density increased with a larger PS concentration, and the cells displayed a spreading morphology on the hybrid films, which promoted cell proliferation. Impressively, cellular stiffness could also be modulated simply by tuning the concentration of nano-spheres. Our results indicate that the addition of PS can effectively tailor the physical and biological properties of PEGDA as well as the mechanical properties of cells, with benefits for biomedical and biotechnological applications.

  18. Evaluation of removal of model particulate and oily soils from poly(ethylene terephthalate) films by microscopic image analysis.

    PubMed

    Gotoh, Keiko; Yu, Nagai; Tagawa, Yumiko

    2013-01-01

    The soil removal behavior from poly(ethylene terephthalate) (PET) films was investigated using a microscopic image analysis system. Carbon black or stearic acid as a model soil was deposited onto a PET film. The PET film was cleaned in various aqueous and non-aqueous solutions by applying stirring or frequency-modulated ultrasound as a mechanical action of soil removal. The amounts of soil deposited on the PET film before and after cleaning were obtained via binary processing of microscopic images, from which the removal efficiency was calculated. Most of the carbon black was deposited on the PET film as submicron aggregates and ultrasound removed them efficiently in a short time, even for relatively smaller aggregates. The removal efficiencies with stirring were less than ca. 10% in all solutions, whereas the removal using ultrasound had high efficiencies that exceeded 80% in the surfactant-free systems. In the case of stearic acid, the removal efficiency with stirring was below 30% in the aqueous solutions, although stearic acid was removed completely in ethanol and n-decane. For ultrasonic cleaning, the removal efficiencies of stearic acid in aqueous solutions became 2-3 times as large as those with the stirring action. To improve soil release in aqueous solutions, the PET film was treated by the dry processing using an atmospheric pressure plasma jet (APPJ) equipment. The wettability and the surface free energy of the PET film were found to increase due to surface oxidation via the APPJ treatment, which resulted in enhanced removal of carbon black and stearic acid in any aqueous solutions.

  19. Analysis of long-term degradation behaviour of polyethylene mulching films with pro-oxidants under real cultivation and soil burial conditions.

    PubMed

    Briassoulis, Demetres; Babou, Epifaneia; Hiskakis, Miltiadis; Kyrikou, Ioanna

    2015-02-01

    Apart from the conventional polyethylene and the bio-based or mainly bio-based biodegradable in soil mulching films, polyethylene mulching films of controlled degradation in soil are already used in agriculture. The use of special pro-oxidants as additives is expected to accelerate the abiotic oxidation and the subsequent chain scission of the polymer under specific UV radiation or thermal degradation conditions, according to the literature. The role of pro-oxidants in the possible biodegradation of polyethylene has been theoretically supported through the use of controlled laboratory conditions. However, results obtained in real soil conditions, but also several laboratory test results, are not supporting these claims and the issue remains disputed. Mulching films made of linear low-density polyethylene (LLDPE) with pro-oxidants, after being used for one cultivation period in an experimental field with watermelon cultivation, were buried in the soil under real field conditions. This work presents the analysis of the degradation of the mulching films during the cultivation period as compared to the corresponding changes after a long soil burial period of 8.5 years. The combined effects of critical factors on the photochemical degradation of the degradable mulching LLDPE films with pro-oxidants under the cultivation conditions and their subsequent further degradation behaviour in the soil are analysed by testing their mechanical properties and through spectroscopic and thermal analysis.

  20. Effects of L-arginine immobilization on the anticoagulant activity and hemolytic property of polyethylene terephthalate films

    NASA Astrophysics Data System (ADS)

    Liu, Yun; Yang, Yun; Wu, Feng

    2010-04-01

    Surface modification of polyethylene terephthalate (PET) films was performed with L-arginine ( L-Arg) to gain an improved anticoagulant surface. The surface chemistry changes of modified films were characterized by X-ray photoelectron spectroscopy (XPS) and attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy. The in vitro anticoagulant activities of the surface-modified PET films were evaluated by blood clotting test, hemolytic test, and the measurement of clotting time including plasma recalcification time (PRT), activated partial thromboplastin time (APTT), and prothrombin time (PT). The data of blood coagulation index (BCI) for L-arginine modified PET films (PET-Arg) was larger than that for PET at the same blood-sample contact time. The hemolysis ratio for PET-Arg was less than that for PET and within the accepted standard for biomaterials. The PRT and APTT for PET-Arg were significantly prolonged by 189 s and 25 s, respectively, compared to those for the unmodified PET. All results suggested that the currently described modification method could be a possible candidate to create antithrombogenic PET surfaces which would be useful for further medical applications.

  1. Evaluation of the stability of nonfouling ultrathin poly(ethylene glycol) films for silicon-based microdevices.

    PubMed

    Sharma, Sadhana; Johnson, Robert W; Desai, Tejal A

    2004-01-20

    The creation of nonfouling surfaces is one of the major prerequisites for microdevices for biomedical and analytical applications. Poly(ethylene glycol) (PEG), a water soluble, nontoxic, and nonimmunogenic polymer has the unique ability of reducing nonspecific protein adsorption and cell adhesion and, therefore, is generally coupled with a wide variety of surfaces to improve their biocompatibility. The performance of these modified surfaces for long-term biomedical applications largely depends on the stability of these PEG films. To this end, we have investigated the stability of covalently coupled ultrathin PEG films on silicon in aqueous in vivo like conditions for a period of 4 weeks. The PEG-modified silicon substrates were incubated in PBS (37 degrees C, pH 7.4, 5% CO2) for different periods of time and then characterized using the techniques of ellipsometry, contact angle measurement, X-ray photoelectron spectroscopy, and atomic force microscopy. The ability of the PEG-modified surfaces to control protein fouling was examined by protein adsorption studies using fluorescein isothiocyanate labeled bovine serum albumin and ellipsometry. Furthermore, the ability of these films to control fibroblast adhesion was examined. Studies suggest that the PEG-modified surfaces retain their protein and cell repulsive nature even though the PEG film thickness decreases for the period of investigation.

  2. Nd:YVO4 laser direct ablation of indium tin oxide films deposited on glass and polyethylene terephthalate substrates.

    PubMed

    Wang, Jian-Xun; Kwon, Sang Jik; Han, Jae-Hee; Cho, Eou Sik

    2013-09-01

    A Q-switched diode-pumped neodymium-doped yttrium vanadate (Nd:YVO4, lambda = 1064 nm) laser was applied to obtain the indium tin oxide (ITO) patterns on flexible polyethylene terephthalate (PET) substrate by a direct etching method. After the ITO films were deposited on a soda-lime glass and PET substrate, laser ablations were carried out on the ITO films for various conditions and the laser ablated results on the ITO films were investigated and analyzed considering the effects of substrates on the laser etching. The laser ablated widths on ITO deposited on glass were found to be much narrower than those on ITO deposited on PET substrate, especially, at a higher scanning speed of laser beam such as 1000 mm/s and 2000 mm/s. As the thermal conductivity of glass substrate is about 7.5 times higher than that of PET, more thermal energy would be spread and transferred to lateral direction in the ITO film in case of PET substrate.

  3. A dual enzyme system composed of a polyester hydrolase and a carboxylesterase enhances the biocatalytic degradation of polyethylene terephthalate films.

    PubMed

    Barth, Markus; Honak, Annett; Oeser, Thorsten; Wei, Ren; Belisário-Ferrari, Matheus R; Then, Johannes; Schmidt, Juliane; Zimmermann, Wolfgang

    2016-08-01

    TfCut2 from Thermobifida fusca KW3 and the metagenome-derived LC-cutinase are bacterial polyester hydrolases capable of efficiently degrading polyethylene terephthalate (PET) films. Since the enzymatic PET hydrolysis is inhibited by the degradation intermediate mono-(2-hydroxyethyl) terephthalate (MHET), a dual enzyme system consisting of a polyester hydrolase and the immobilized carboxylesterase TfCa from Thermobifida fusca KW3 was employed for the hydrolysis of PET films at 60°C. HPLC analysis of the reaction products obtained after 24 h of hydrolysis showed an increased amount of soluble products with a lower proportion of MHET in the presence of the immobilized TfCa. The results indicated a continuous hydrolysis of the inhibitory MHET by the immobilized TfCa and demonstrated its advantage as a second biocatalyst in combination with a polyester hydrolase for an efficient degradation oft PET films. The dual enzyme system with LC-cutinase produced a 2.4-fold higher amount of degradation products compared to TfCut2 after a reaction time of 24 h confirming the superior activity of his polyester hydrolase against PET films.

  4. Highly hydrophilic ultra-high molecular weight polyethylene powder and film prepared by radiation grafting of acrylic acid

    NASA Astrophysics Data System (ADS)

    Wang, Honglong.; Xu, Lu.; Li, Rong.; Pang, Lijuan.; Hu, Jiangtao.; Wang, Mouhua.; Wu, Guozhong.

    2016-09-01

    The surface properties of ultra-high molecular weight polyethylene (UHMWPE) are very important for its use in engineering or composites. In this work, hydrophilic UHMWPE powder and film were prepared by γ-ray pre-irradiation grafting of acrylic acid (AA) and further neutralization with sodium hydroxide solution. Variations in the chemical structure, grafting yield and hydrophilicity were investigated and compared. FT-IR and XPS analysis results showed that AA was successfully grafted onto UHMWPE powder and film; the powder was more suitable for the grafting reaction in 1 wt% AA solution than the film. Given a dose of 300 kGy, the grafting yield of AA was ∼5.7% for the powder but ∼0.8% for the film under identical conditions. Radiation grafting of a small amount of AA significantly improved the hydrophilicity of UHMWPE. The water contact angle of the UHMWPE-g-PAA powder with a grafting yield of AA at ∼5.7% decreased from 110.2° to 68.2°. Moreover, the grafting powder (UHMWPE-g-PAA) exhibited good dispersion ability in water.

  5. ESCA Study of Poly (Vinylidene Fluoride) Tetrafluoroethylene - Ethylene Copolymer and Polyethylene Exposed to Atomic Oxygen

    NASA Technical Reports Server (NTRS)

    Golub, Morton A.; Cormia, Robert D.

    1989-01-01

    The ESCA (electron spectroscopy for chemical analysis) spectra of films of poly(vinylidene fluoride) (PVDF), tetrafluoroethylene-ethylene copolymer (TFE/ET) and polyethylene (PE) exposed to atomic oxygen (O(P-3)), in or out of the glow of a radio-frequency O2 plasma, were compared. ESCA spectra of PE films exposed to (O(P-3)) in low Earth orbit (LEO) on the STS-8 Space Shuttle were also examined. Apart from O(P-3)-induced surface recession (etching), the various polymer films exhibited surface oxidation, which proceeded towards equilibrium saturation oxygen levels. The maximum surface oxygen uptakes for in-glow or out-of-glow exposures were in the order: PE greater than TFE/ET greater than PVDF; for PE itself, the oxygen uptakes were in the order: in glow greater than out of glow greater than LEO. Given prior ESCA data on poly(vinyl fluoride) and polytetrafluoroethylene films exposed to O(P-3), the extent of surface oxidation is seen to decrease regularly with increase in fluorine substitution in a family of ethylene-type polymers. (Keywords: ESCA; poly(vinylidene fluoride); tetrafluoroethylene ethylene copolymer; polyethylene; atomic oxygen; radio-frequency oxygen plasma; low Earth orbit)

  6. Characterization of polyester films used in capacitors. 2: Effects of heat treatments on transient and steady-state charging currents in polyethylene terephthalate thin films

    NASA Astrophysics Data System (ADS)

    Thielen, A.; Cerfontaine, J.; Niezette, J.; Feyder, G.; Vanderschueren, J.

    1994-10-01

    The effects of various heat treatments performed before or after the vacuum deposition of aluminum electrodes on the charging currents flowing through polyethylene terephthalate (PET) thin films (6 and 12 micrometers) were studied. The amorphous phase of the PET films was characterized by the use of thermally stimulated current/relaxation map analysis spectrometry, allowing precise determination of thermodynamic and thermokinetic parameters. Density measurements were used to calculate the rate of crystallinity achieved after annealing. A correlation was found between the relaxation parameters of the alpha dipolar relaxation of PET, the rate of crystallinity, and the properties of the charging currents observed from room temperature to 200 C. Strain-induced crystallization has been put forward to account for the experimental evidences.

  7. 77 FR 14493 - Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic of China: Final...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-03-12

    ..., and strip (``PET film'') from the People's Republic of China (``PRC'').\\1\\ The period of review (``POR... administrative review of PET film from the People's Republic of China.\\2\\ On November 28, 2011, DuPont Teijin... raw, pre- treated, or primed PET film, whether extruded or co-extruded. Excluded are metalized...

  8. Deformation mechanism in swollen radiation-grafted polyethylene

    NASA Astrophysics Data System (ADS)

    Ungar, G.; Dlugosz, J.; Ranogajec, F.

    Stress-strain behaviour of anisotropic polyethylene (PE) film radiation-grafted with styrene was studied with the samples immersed in xylene. The glassy polystyrene (PS) phase (1) is softened by swelling. Whereas the tensile modulus of dry graft increases somewhat with increasing PS content, for the swollen graft it decreases sharply. However the yield stress and the elongation at break remain fairly large. For highly grafted films (PS/PE > 1) deformation is almost fully reversible and proceeds without necking up to draw ratios as high as 5:1. With the aid of additional X-ray diffraction and transmission electron microscopy results the deformation mechanism is interpreted in terms of the known morphology of the copolymer.

  9. Evaluation of various polyethylene as potential dosimeters by attenuated total reflectance-Fourier-transform infrared spectroscopy

    NASA Astrophysics Data System (ADS)

    Halperin, Fred; Collins, Greta; DiCicco, Michael; Logar, John

    2014-12-01

    Various types of polyethylene (PE) have been evaluated in the past for use as a potential dosimeter, chiefly via the formation of an unsaturated transvinylene (TV) double-bond resulting from exposure to ionizing radiation. The utilization of attenuated total reflectance Fourier-transform infrared (ATR-FTIR) spectroscopy in characterizing TV formation in irradiated PE for a potential dosimeter has yet to be fully developed. In this initial investigation, various PE films/sheets were exposed to ionizing radiation in a high-energy 5 megaelectron volt (MeV) electron beam accelerator in the 10-500 kilogray (kGy) dose range, followed by ATR-FTIR analysis of TV peak formation at the 965 cm-1 wavenumber. There was an upward trend in TV formation for low-density polyethylene (LDPE) films and high-density polyethylene (HDPE) sheets as a function of absorbed dose in the 10-50 kGy dose range, however, the TV response could not be equated to a specific absorbed dose. LDPE film displayed a downward trend from 50 kGy to 250 kGy and then scattering up to 500 kGy; HDPE sheets demonstrated an upward trend in TV formation up to 500 kGy. For ultra-high molecular weight polyethylene (UHMWPE) sheets irradiated up to 150 kGy, TV response was equivalent to non-irradiated UHMWPE, and a minimal upward trend was observed for 200 kGy to 500 kGy. The scatter of the data for the irradiated PE films/sheets is such that the TV response could not be equated to a specific absorbed dose. A better correlation of the post-irradiation TV response to absorbed dose may be attained through a better understanding of variables.

  10. Mechanically Robust and Transparent N-Halamine Grafted PVA-co-PE Films with Renewable Antimicrobial Activity.

    PubMed

    Si, Yang; Cossu, Andrea; Nitin, Nitin; Ma, Yue; Zhao, Cunyi; Chiou, Bor-Sen; Cao, Trung; Wang, Dong; Sun, Gang

    2017-03-01

    Antimicrobial polymeric films that are both mechanically robust and function renewable would have broad technological implications for areas ranging from medical safety and bioengineering to foods industry; however, creating such materials has proven extremely challenging. Here, a novel strategy is reported to create high-strength N-halamine incorporated poly(vinyl alcohol-co-ethylene) films (HAF films) with renewable antimicrobial activity by combining melt radical graft polymerization and reactive extrusion technique. The approach allows here the intrinsically rechargeable N-halamine moieties to be covalently incorporated into polymeric films with high biocidal activity and durability. The resulting HAF films exhibit integrated properties of robust mechanical strength, high transparency, rechargeable chlorination capability (>300 ppm), and long-term durability, which can effectively offer 3-5 logs CFU reduction against typical pathogenic bacterium Escherichia coli within a short contact time of 1 h, even at high organism conditions. The successful synthesis of HAF films also provides a versatile platform for exploring the applications of antimicrobial N-halamine moieties in a self-supporting, structurally adaptive, and function renewable form.

  11. Efficacy of two acidic sanitizers for microbial reduction on metal cans and low-density polyethylene film surfaces.

    PubMed

    Lee, J; Gupta, M J; Lopes, J; Pascall, M A

    2007-10-01

    This study investigated 2 sanitizer formulations and compared them with hydrogen peroxide (H(2)O(2)). Formulation number 1 contained citric acid and sodium dodecylbenzene sulfonate (SDBS). Formulation number 2 contained SDBS, citric, lactic, phosphoric acids, and benzoic acid. Low concentration levels of the sanitizers (1.0% for formulation 1 and 0.5% for formulation 2) were compared with 35% H(2)O(2) for their efficacies on Escherichia coli, Listeria innocua, and Saccharomyces cerevisiae inoculated onto low-density polyethylene (LDPE) films and metal cans at room temperature (23 +/- 1 degrees C) and 40 degrees C. The results showed that both formulations 1 and 2 required >120 s to sanitize both materials from microbial populations at room temperature, while <15 s was needed for the H(2)O(2). Except for formulation 1 on the E. coli inoculated LDPE film surface, the sanitizers completely eliminated the bacterial populations on both materials in 60 s at 40 degrees C. In general, the formulations were more effective for reduction of the microbial numbers on the can material when compared with the LDPE film. The E. coli showed greater tolerance for the sanitizers when exposed to the process conditions in this study. All sanitizers completely eliminated the test organisms in

  12. Enhancing distributive mixing of immiscible polyethylene/thermoplastic starch blend through zeolite ZSM-5 compounding sequence.

    PubMed

    Thipmanee, Ranumas; Lukubira, Sam; Ogale, Amod A; Sane, Amporn

    2016-01-20

    The aim of this work was to explore the effect of zeolite ZSM-5 (ZSM5) incorporation sequence on the phase morphology, microstructure, and performance of polyethylene/thermoplastic starch (PE/TPS) films. Two processing sequences were used for preparing PE/TPS/ZSM5 composites at a weight ratio of PE to TPS of 70:30 and ZSM5 concentrations of 1-5 wt%: (i) melt compounding of PE with ZSM5 prior to melt blending with TPS (SI); and (ii) TPS was compounded with ZSM5 prior to blending with PE (SII). Distributive mixing and mechanical properties of PE/TPS blend were greatly enhanced when ZSM5 was incorporated via SII. These were caused by both the higher affinity between PE and ZSM5, compared to that of TPS and ZSM5, and the reduction of TPS viscosity after compounding with ZSM5, leading to migration of ZSM5 from TPS dispersed phase toward PE matrix and increase in breakup of TPS droplets during SII sequence.

  13. Construction of antibacterial poly(ethylene terephthalate) films via layer by layer assembly of chitosan and hyaluronic acid.

    PubMed

    Del Hoyo-Gallego, Sara; Pérez-Álvarez, Leyre; Gómez-Galván, Flor; Lizundia, Erlantz; Kuritka, Ivo; Sedlarik, Vladimir; Laza, Jose Manuel; Vila-Vilela, Jose Luis

    2016-06-05

    Polyelectrolytic multilayers (PEMs) with enhanced antibacterial properties were built up onto commercial poly(ethylene terephthalate) (PET) films based on the layer by layer assembling of bacterial contact killing chitosan and bacterial repelling highly hydrated hyaluronic acid. The optimization of the aminolysis modification reaction of PET was carried out by the study of the mechanical properties and the surface characterization of the modified polymers. The layer by layer assembly was successfully monitored by TEM microscopy, surface zeta-potential, contact angle measurements and, after labeling with fluorescein isothiocyanate (FTIC) by absorption spectroscopy and confocal fluorescent microscopy. Beside, the stability of the PEMs was studied at physiological conditions in absence and in the presence of lysozyme and hyaluronidase enzymes. Antibacterial properties of the obtained PEMs against Escherichia coli were compared with original commercial PET.

  14. Preparation of a high-density polyethylene (HDPE) film with a nucleating agent during a stretching process

    NASA Astrophysics Data System (ADS)

    Park, Jong-Seok; Cho, In-Hee; Gwon, Sung-Jin; Lim, Youn-Mook; Nho, Young-Chang

    2009-07-01

    The effects of the crystallinity and a radiation crosslinking on the high-density polyethylene (HDPE) with a nucleating agent were investigated. We found the optimum conditions for the stretching process according to the addition of various quantities of a nucleating agent (Millad3988). The pores of a HDPE membrane were affected by the crystallinity of the polymer, and the crystallinity of the polymer was changed with an increase thermal ageing temperature. Thermal ageing treatment of the HDPE film was conducted in an oven at 110-135 °C for 5-60 min. When the conditions for the annealing were fixed at 125 °C and 40 min, we obtained the highest crystallinity. Also, the resulting mechanical properties of the irradiated HDPE separators were analyzed.

  15. Improvement of barrier properties of rotomolded PE containers with nanoclay

    SciTech Connect

    Jamshidi, Shadi; Sundararaj, Uttandaraman

    2015-05-22

    Polyethylene (PE) is widely used to make bulk containers in rotational molding process. The challenge in this study is to improve permeation resistance of PE to hydrocarbon solvents and gases. Adding organomodified clay improves the thermal, barrier and mechanical properties of PE. In fact, clay layers create a tortuous path against the permeant, yielding better barrier properties. Due to the non-polar hydrophobic nature of PE and polar hydrophilic structure of clay minerals, the compatibilizer plays a crucial role to enhance the dispersion level of clay in the matrix. In this study High Density Polyethylene (HDPE) and Linear Low Density Polyethylene (LLDPE) layered silicate nanocomposite were melt-compounded with two concentrations of organomodified clay (2 and 4 wt. %). The interaction between nanoclay, compatibilizer and rotomolding grade of PE were examined by using X-ray diffraction, transmission electron microscopy (TEM) and rheology test. Rheology was used to determine the performance of our material at low shear processing condition.

  16. Improvement of barrier properties of rotomolded PE containers with nanoclay

    NASA Astrophysics Data System (ADS)

    Jamshidi, Shadi; Sundararaj, Uttandaraman

    2015-05-01

    Polyethylene (PE) is widely used to make bulk containers in rotational molding process. The challenge in this study is to improve permeation resistance of PE to hydrocarbon solvents and gases. Adding organomodified clay improves the thermal, barrier and mechanical properties of PE. In fact, clay layers create a tortuous path against the permeant, yielding better barrier properties. Due to the non-polar hydrophobic nature of PE and polar hydrophilic structure of clay minerals, the compatibilizer plays a crucial role to enhance the dispersion level of clay in the matrix. In this study High Density Polyethylene (HDPE) and Linear Low Density Polyethylene (LLDPE) layered silicate nanocomposite were melt-compounded with two concentrations of organomodified clay (2 and 4 wt. %). The interaction between nanoclay, compatibilizer and rotomolding grade of PE were examined by using X-ray diffraction, transmission electron microscopy (TEM) and rheology test. Rheology was used to determine the performance of our material at low shear processing condition.

  17. Efficient and selective degradation of polyethylenes into liquid fuels and waxes under mild conditions.

    PubMed

    Jia, Xiangqing; Qin, Chuan; Friedberger, Tobias; Guan, Zhibin; Huang, Zheng

    2016-06-01

    Polyethylene (PE) is the largest-volume synthetic polymer, and its chemical inertness makes its degradation by low-energy processes a challenging problem. We report a tandem catalytic cross alkane metathesis method for highly efficient degradation of polyethylenes under mild conditions. With the use of widely available, low-value, short alkanes (for example, petroleum ethers) as cross metathesis partners, different types of polyethylenes with various molecular weights undergo complete conversion into useful liquid fuels and waxes. This method shows excellent selectivity for linear alkane formation, and the degradation product distribution (liquid fuels versus waxes) can be controlled by the catalyst structure and reaction time. In addition, the catalysts are compatible with various polyolefin additives; therefore, common plastic wastes, such as postconsumer polyethylene bottles, bags, and films could be converted into valuable chemical feedstocks without any pretreatment.

  18. Efficient and selective degradation of polyethylenes into liquid fuels and waxes under mild conditions

    PubMed Central

    Jia, Xiangqing; Qin, Chuan; Friedberger, Tobias; Guan, Zhibin; Huang, Zheng

    2016-01-01

    Polyethylene (PE) is the largest-volume synthetic polymer, and its chemical inertness makes its degradation by low-energy processes a challenging problem. We report a tandem catalytic cross alkane metathesis method for highly efficient degradation of polyethylenes under mild conditions. With the use of widely available, low-value, short alkanes (for example, petroleum ethers) as cross metathesis partners, different types of polyethylenes with various molecular weights undergo complete conversion into useful liquid fuels and waxes. This method shows excellent selectivity for linear alkane formation, and the degradation product distribution (liquid fuels versus waxes) can be controlled by the catalyst structure and reaction time. In addition, the catalysts are compatible with various polyolefin additives; therefore, common plastic wastes, such as postconsumer polyethylene bottles, bags, and films could be converted into valuable chemical feedstocks without any pretreatment. PMID:27386559

  19. Minimizing photooxidation in pasteurized milk by optimizing light transmission properties of green polyethylene films.

    PubMed

    Intawiwat, N; Wold, J P; Skaret, J; Rukke, E O; Pettersen, M K

    2013-01-01

    The effect of different amounts of transmitted green light on photooxidation in pasteurized milk was studied. Five different green films produced with combinations of pigments and additives to minimize exposure to harmful wavelengths with regard to photosensitizers (400-450 and 600-650 nm) were evaluated. In addition, a non-colored transparent film and an orange film were compared with 1 selected green film. Pasteurized milk (3.9% fat) was packed in an air atmosphere and exposed to light for 14, 20, 26, and 32 h at 4 °C under the different films. Samples stored in the dark were control samples. The results showed that the most-effective green film had low overall light transmission, and also almost completely blocked light wavelengths shorter than 450 nm and wavelengths longer than 600 nm, which prevented photooxidation of riboflavin and chlorophyllic compounds. Chlorophyll degradation was highly correlated with sensory properties (coefficient of determination = 0.80-0.94). To preserve milk quality, total blocking of all visible light would be preferable. If total blocking is not feasible, then light transmission for wavelength below 450 nm and above 650 nm should be minimized (e.g., less than 5%). The newly developed green film can be used as a prototype for protection of dairy products to reduce the degradation of photosensitizers.

  20. Spray coating of carbon nanotube on polyethylene terephthalate film for touch panel application.

    PubMed

    Park, Chul; Kim, Seok Won; Lee, Yun-Su; Lee, Sung Ho; Song, Kyu Ho; Park, Lee Soon

    2012-07-01

    From a technical perspective, the major limiting factors for the wide adoption of CNT films are the DC conductivity, uniformity of sheet resistance and good adhesion of CNT on film substrate. In this study, the effects of sonificator and process time on the zeta potential and sheet resistance of the CNT-PET film show that although the dispersing power of horn-type sonificator is stronger than that of bath-type, the SWCNT solution obtained with horn-type sonificator agglomerates faster. Likewise, it has been noted that the SWCNT solutions with low enough zeta potentials exhibit higher sheet resistance after making CNT-PET films due to the damage to SWCNTs caused by high dispersion force. Since the spray coating of SWCNT solution gives the SWCNT-SDS composite layer on PET film after drying, the excess SDS should be washed off. The removal of excess SDS was conducted by dipping in the 3 N HNO3 and SOCl2 solution and washing with deionized water followed by heat treatment in a 120 degrees C convection oven for 30 min. The lift-off of SWCNT-SDS composite layer after 40 min dipping in the 3 N HNO3 solution appeared to be due to the continued permeation leading to swelling of the SDS layer by the 3 N HNO3 aqueous solution. It was found that ten times of spray coating cycle gave CNT-PET film the sheet resistance of 310 Ω/[square] and transmittance of 81%. The TSP made with CNT-PET film exhibited a performance equal to the one made with ITO-PET film.

  1. Tuning thin-film electrolyte for lithium battery by grafting cyclic carbonate and combed poly(ethylene oxide) on polysiloxane.

    PubMed

    Li, Jie; Lin, Yue; Yao, Hehua; Yuan, Changfu; Liu, Jin

    2014-07-01

    A tunable polysiloxane thin-film electrolyte for all-solid-state lithium-ion batteries was developed. The polysiloxane was synthesized by hydrosilylation of polymethylhydrosiloxane with cyclic [(allyloxy)methyl]ethylene ester carbonic acid and vinyl tris(2-methoxyethoxy)silane. (1) H NMR spectroscopy and gel-permeation chromatography demonstrated that the bifunctional groups of the cyclic propylene carbonate (PC) and combed poly(ethylene oxide) (PEO) were well grafted on the polysiloxane. At PC/PEO=6:4, the polysiloxane-based electrolyte had an ionic conductivity of 1.55 × 10(-4) and 1.50 × 10(-3)  S cm(-1) at 25 and 100 °C, respectively. The LiFePO4 /Li batteries fabricated with the thin-film electrolyte presented excellent cycling performance in the temperature range from 25 to 100 °C with an initial discharge capacity at a rate of 1 C of 88.2 and 140 mA h g(-1) at 25 and 100 °C, respectively.

  2. Effect of stearic acid-grafted starch compatibilizer on properties of linear low density polyethylene/thermoplastic starch blown film.

    PubMed

    Khanoonkon, Nattaporn; Yoksan, Rangrong; Ogale, Amod A

    2016-02-10

    The present work aims to investigate the effect of stearic acid-grafted starch (ST-SA) on the rheological, thermal, optical, dynamic mechanical thermal, and tensile properties of linear low density polyethylene/thermoplastic starch (LLDPE/TPS) blends, as well as on their water vapor and oxygen barrier properties. Blends consisting of LLDPE and TPS in a weight ratio of 60:40 and ST-SA at different concentrations, i.e. 1, 3 and 5%, were prepared using a twin-screw extruder. The obtained resins were subsequently converted into films via blown film extrusion. Incorporation of ST-SA resulted in a decreased degree of shear thinning, reduced ambient temperature elasticity, and improved tensile strength, secant modulus, extensibility, and UV absorption, as well as diminished water vapor and oxygen permeabilities of the LLDPE/TPS blend. These effects are attributed to the enhanced interfacial adhesion between LLDPE and TPS phases through the compatibilizing effect induced by ST-SA, and the good dispersion of the TPS phase in the LLDPE matrix. The results confirmed that ST-SA could potentially be used as a compatibilizer for the LLDPE/TPS blend system.

  3. Antifouling properties of poly(methyl methacrylate) films grafted with poly(ethylene glycol) monoacrylate immersed in seawater.

    PubMed

    Iguerb, O; Poleunis, C; Mazéas, F; Compère, C; Bertrand, P

    2008-11-04

    Biofouling of all structures immersed in seawater constitutes an important problem, and many strategies are currently being developed to tackle it. In this context, our previous work shows that poly(ethylene glycol) monoacrylate (PEGA) macromonomer grafted on preoxidized poly(methyl methacrylate) (PMMAox) films exhibits an excellent repellency against the bovine serum albumin used as a model protein. This study aims to evaluate the following: (1) the prevention of a marine extract material adsorption by the modified surfaces and (2) the antifouling property of the PEGA-g-PMMAox substrates when immersed in natural seawater during two seasons (season 1: end of April-beginning of May 2007, and season 2: end of October-beginning of November 2007). The antifouling performances of the PEGA-g-PMMAox films are investigated for different PEG chain lengths and macromonomer concentrations into the PEGA-based coatings. These two parameters are followed as a function of the immersion time, which evolves up to 14 days. The influence of the PEGA layer on marine compounds (proteins and phospholipids) adsorption is evidenced by time-of-flight secondary ion mass spectrometry (ToF-SIMS) and X-ray photoelectron spectroscopy (XPS). It was found that the antifouling efficiency of the PEGA-grafted surfaces increases with both PEGA concentration and PEG chain length.

  4. Characterization of polyelectrolyte multilayer films on polyethylene terephtalate vascular prostheses under mechanical stretching.

    PubMed

    Rinckenbach, Simon; Hemmerlé, Joseph; Dieval, Florence; Arntz, Youri; Kretz, Jean-Georges; Durand, Bernard; Chakfe, Nabil; Schaaf, Pierre; Voegel, Jean-Claude; Vautier, Dominique

    2008-03-01

    Layer-by-layer (LBL) polyelectrolyte films offer extensive potentials to enhance surface properties of vascular biomaterials. From the time of implantation, PET prostheses are continuously subjected to multiple mechanical stresses such as important distorsions and blood pressure. In this study, three LBL films, namely (1) poly(sodium 4-styrenesulfonate)/poly(allylamine hydrochloride), (2) poly(L-lysine)/hyaluronan, and (3) poly(L-lysine)/poly(L-glutamic acid) were built on to isolated PET filaments, thread, and vascular prostheses. The three LBL films uniformly covered the surface of the PET samples with rough, totally smooth, and "wrinkled" appearances respectively for (PAH/PSS)(24), (PLL/HA)(24), and (PLL/PGA)(24) systems. We then assessed the behavior of these LBL films, in an aqueous environment [by environmental scanning electronic microscopy (ESEM)], when subjected to unidirectional longitudinal stretches. We found that stretching induces ruptures in the multilayer films on isolated filaments for longitudinal stretches of 14% for (PSS/PAH)(24), 13% for (PLL/PGA)(24), and 30% for (PLL/HA)(24) films. On threads, the rupture limit is enhanced to be respectively 26, 20, and 28%. Most interestingly, we found that on vascular prosthesis no rupture is visible in any of the three multilayers types, even for elongations of 200% (200% undergone by the PET prostheses is representative of those encountered during graft deployment) which by far exceeds elongations observed under physiological conditions (10-20%, blood pressure). In term of mechanical behaviors, these preliminary data constitute a first step toward the possible use of LBL film to coat and functionalize vascular prosthesis.

  5. Material characterization and thermoforming of polyethylene terephthalate film for electrical insulation: Topical report

    SciTech Connect

    Carey, D.A.; Smith, B.P.

    1987-12-01

    Differential scanning calorimetry (DSC) was used to determine as-received glass transition, crystallization, and melting temperatures of polyethylene terephthalate (PET). A Box-Behnken statistical designed experiment was used to evaluate the effect of forming temperature, forming rate, and heat-set temperature on shrinkage, tear resistance, and thermal properties. At a forming temperature of 88/sup 0/C and heat-set temperature of 180/sup 0/C, good-quality PET parts were produced. The optimum forming time appears to be either 0.5 min or 5.0 min. In addition, inductively coupled argon plasma emission spectroscopy (ICAP) was used to determine the catalyst system for both PET sheets from two vendors.

  6. Hydrophilic polysulfone film prepared from polyethylene glycol monomethylether via coupling graft

    NASA Astrophysics Data System (ADS)

    Du, Ruikui; Gao, Baojiao; Li, Yanbin

    2013-06-01

    In the presence of acid-acceptor Na2CO3, the nucleophilic substitution between chloromethylated polysulfone (CMPSF) and polyethylene glycol monomethylether (PEGME) was conducted. Polyethylene glycol (PEG) was coupling-grafted onto the side chains of polysulfone (PSF) so that the graft copolymer PSF-g-PEG was prepared and the hydrophilic modification of polysulfone membrane material was realized. The chemical structure of PSF-g-PEG was characterized by FTIR and 1H NMR. The influence of the main factors on the coupling graft reaction was investigated. The water static contact angle of PSF-g-PEG membrane was determined and its property of resisting protein pollution was examined by using bovine serum albumin (BSA) as a model protein. The experimental results show that the coupling graft reaction between CMPSF and PEGME can proceed successfully, and the reaction of chloromethyl groups of CMPSF with the hydroxyl end groups of PEGME is a typical SN1 nucleophilic substitution reaction. The polarity of the solvents and the reaction temperature greatly influence the reaction. The suitable solvent is dimethyl acetamide with stronger polarity and 70 °C is a suitable reaction temperature. After reaction of 36 h, the grafting degree of PEG can reach 48 g/100 g and the product yield is about 73.6%. The contact angle of PSF-g-PEG membrane declines rapidly with the increase of PEG grafting degree, displaying the obvious enhancement of the hydrophilicity. The adsorption capacity of BSA on PSF-g-PEG membrane decreases remarkably with the increase of PEG grafting degree, showing excellent antifouling ability of PSF-g-PEG membrane for proteins.

  7. 21 CFR 172.260 - Oxidized polyethylene.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Oxidized polyethylene. 172.260 Section 172.260 Food... Coatings, Films and Related Substances § 172.260 Oxidized polyethylene. Oxidized polyethylene may be safely used as a component of food, subject to the following restrictions: (a) Oxidized polyethylene is...

  8. Spectroscopic studies of Cr{sup 3+} ions doped in poly(vinylalcohol) complexed polyethylene glycol polymer films

    SciTech Connect

    Rao, T. Rajavardhana; Raju, Ch. Linga; Brahmam, K. Veera

    2015-05-15

    Polymer films of Poly(vinylalcohol) (PVA) complexed with Polyethylene glycol (PEG) with different dopant concentrations of Cr{sup 3+} ions are prepared by solution cast technique. Electron paramagnetic resonance (EPR), Optical absorption and FT-IR studies have been carried out on the polymer films. The EPR spectra of the entire samples exhibit resonance signal at g ≈1.97 which is attributed to the isolated Cr{sup 3+} pairs. The temperature variation EPR studies show that the population of spin-levels participating in the resonance decreases with an increase in temperature, which is in accordance with the Boltzmann Law. The paramagnetic susceptibilities (X) have been calculated from the EPR data at different temperatures. The linewidth of the g ≈1.97 resonance signal has been found to be decreasing with an increase in temperature, which confirms the pairing mechanism between Cr{sup 3+} ions. The Optical absorption spectrum of chromium ions in (PVA+PEG) polymer films exhibits three bands, corresponding to the d-d transitions {sup 4}A{sub 2g}(F)→{sup 4}T{sub 1g}(F), {sup 4}A{sub 2g}(F)→{sup 4}T{sub 2g}(F) and {sup 4}A{sub 2g}(F)→{sup 2}T{sub 1g}(G), in the order of decreasing energy. The crystal field parameter Dq and the Racah interelectronic repulsion parameters B and C have been evaluated. From the ultraviolet absorption edges, Optical band gap (E{sub opt}) and Urbach (ΔE) energies are evaluated. FT-IR spectrum exhibits few bands which are attributed to O-H, CH, C=C and C=O groups of stretching and bending vibrations.

  9. Efficient immobilization and patterning of biomolecules on poly(ethylene terephthalate) films functionalized by ion irradiation for biosensor applications.

    PubMed

    Hwang, In-Tae; Kuk, In-Seol; Jung, Chan-Hee; Choi, Jae-Hak; Nho, Young-Chang; Lee, Young-Moo

    2011-07-01

    The surface of a poly(ethylene terephthalate) (PET) film was selectively irradiated with proton beams at various fluences to generate carboxylic acid groups on the surface; the resulting functionalized PET surface was then characterized in terms of its wettability, chemical structure, and chemical composition. The results revealed that (i) carboxylic acid groups were successfully generated in the irradiated regions of the PET surface, and (ii) their relative amounts were dependent on the fluence. A capture biomolecule, anthrax toxin probe DNA, was selectively immobilized on the irradiated regions on the PET surface. Cy3-labeled DNA as a target biomolecule was then hybridized with the probe DNA immobilized on the PET surface. Liver-cancer-specific α-fetoprotein (AFP) antigen, as a target biomolecule, was also selectively immobilized on the irradiated regions on the PET surface. Texas Red-labeled secondary antibody was then reacted with an AFP-specific primary antibody prebound to the AFP antigen on the PET surface for the detection of the target antigen, using an indirect immunoassay method. The results revealed that (i) well-defined micropatterns of biomolecules were successfully formed on the functionalized PET surfaces and (ii) the fluorescence intensity of the micropatterns was dependent mainly on the concentrations of the target DNA hybridized to the probe DNA and the target AFP antigen immobilized on the PET films. The lowest detectable concentrations of the target DNA and target AFP antigen in this study were determined to be 4 and 16 ng/mL, respectively, with the PET film prepared at a fluence of 5 × 10(14) ions/cm(2).

  10. Effect of Tris, MOPS, and phosphate buffers on the hydrolysis of polyethylene terephthalate films by polyester hydrolases.

    PubMed

    Schmidt, Juliane; Wei, Ren; Oeser, Thorsten; Belisário-Ferrari, Matheus Regis; Barth, Markus; Then, Johannes; Zimmermann, Wolfgang

    2016-09-01

    The enzymatic degradation of polyethylene terephthalate (PET) occurs at mild reaction conditions and may find applications in environmentally friendly plastic waste recycling processes. The hydrolytic activity of the homologous polyester hydrolases LC cutinase (LCC) from a compost metagenome and TfCut2 from Thermobifida fusca KW3 against PET films was strongly influenced by the reaction medium buffers tris(hydroxymethyl)aminomethane (Tris), 3-(N-morpholino)propanesulfonic acid (MOPS), and sodium phosphate. LCC showed the highest initial hydrolysis rate of PET films in 0.2 m Tris, while the rate of TfCut2 was 2.1-fold lower at this buffer concentration. At a Tris concentration of 1 m, the hydrolysis rate of LCC decreased by more than 90% and of TfCut2 by about 80%. In 0.2 m MOPS or sodium phosphate buffer, no significant differences in the maximum initial hydrolysis rates of PET films by both enzymes were detected. When the concentration of MOPS was increased to 1 m, the hydrolysis rate of LCC decreased by about 90%. The activity of TfCut2 remained low compared to the increasing hydrolysis rates observed at higher concentrations of sodium phosphate buffer. In contrast, the activity of LCC did not change at different concentrations of this buffer. An inhibition study suggested a competitive inhibition of TfCut2 and LCC by Tris and MOPS. Molecular docking showed that Tris and MOPS interfered with the binding of the polymeric substrate in a groove located at the protein surface. A comparison of the K i values and the average binding energies indicated MOPS as the stronger inhibitor of the both enzymes.

  11. Peel/seal properties of poly(ethylene methyl acrylate)/polybutene-1 blend films

    NASA Astrophysics Data System (ADS)

    Mohammdi, Seyedeh Raziyeh; Ajji, Abdellah; Tabatabaei, Seyed H.

    2015-05-01

    Nowadays, the possibility to easy open a food package is of great interest both from the consumer and food producers' perspective. In this study, the peel/seal properties of poly (ethylene methyl acrylate) (EMA)/polybutene-1 (PB-1) blend films were investigated. Three blends of EMA/PB-1 with different methyl acrylate (MA) content were prepared using cast extrusion process. Differential Scanning Calorimetry (DSC) was used to investigate the thermal behavior as well as the crystalinity of the blends. The effect of polymer matrix on the crystalline structure of PB-1 was studied using Wide Angle X-ray Diffraction (WAXD) and DSC. T-peel tests were carried out on the heat sealed films at various seal temperatures. The effect of MA content and heat seal temperature on peel/seal properties (i.e. peel initiation temperature, temperature window of sealability and peel strength) of the films were studied.

  12. Peel/seal properties of poly(ethylene methyl acrylate)/polybutene-1 blend films

    SciTech Connect

    Mohammdi, Seyedeh Raziyeh; Ajji, Abdellah; Tabatabaei, Seyed H.

    2015-05-22

    Nowadays, the possibility to easy open a food package is of great interest both from the consumer and food producers’ perspective. In this study, the peel/seal properties of poly (ethylene methyl acrylate) (EMA)/polybutene-1 (PB-1) blend films were investigated. Three blends of EMA/PB-1 with different methyl acrylate (MA) content were prepared using cast extrusion process. Differential Scanning Calorimetry (DSC) was used to investigate the thermal behavior as well as the crystalinity of the blends. The effect of polymer matrix on the crystalline structure of PB-1 was studied using Wide Angle X-ray Diffraction (WAXD) and DSC. T-peel tests were carried out on the heat sealed films at various seal temperatures. The effect of MA content and heat seal temperature on peel/seal properties (i.e. peel initiation temperature, temperature window of sealability and peel strength) of the films were studied.

  13. Picosecond UV laser induced scribing of polyethylene terephthalate (PET) films for the enhancement of their flexibility

    NASA Astrophysics Data System (ADS)

    Kang, Min Gi; Kim, Changhwan; Lee, Yong Joong; Kim, Sung Yeol; Lee, Ho

    2016-08-01

    Flexible devices has received a great attention due to their high portability, lightness, and ease of shape reconfiguration. To achieve high flexibility, controlling the mechanical properties of the substrate materials is of importance. In this paper, we controlled the local flexibility of PET films via UV laser scribing. The bending test of the films revealed that their bending curvatures, the associated mechanical damages, and the required bending forces could be successfully tuned by controlling the number and the depth of the scribed lines. Our simple strategy of using laser scribing will find its usefulness in flexible device applications where high flexibility and mechanical stability are required.

  14. 76 FR 47546 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary Results of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-08-05

    ... exporter of PET Film from India. The Department preliminarily determines that Ester did not make sales of..., Ester provided a chart of its selling functions.\\2\\ However, it did not provide a breakout of sales... chart to include the level of degree of the selling activities, but did not break out the...

  15. Complete genome sequence of Bacillus sp. YP1, a polyethylene-degrading bacterium from waxworm's gut.

    PubMed

    Yang, Yu; Chen, Jianwei; Wu, Wei-Min; Zhao, Jiao; Yang, Jun

    2015-04-20

    Bacillus sp. strain YP1, isolated from the gut of waxworm (the larvae of Plodia interpunctella) which ate polyethylene (PE) plastic, is capable of degrading PE and utilizing PE as sole carbon source. Here we report the complete genome sequence of strain YP1, which is relevant to polyethylene depolymerization and biodegradation.

  16. Dissociating space charge processes from orientation polarization in poly(ethylene naphthalate) films

    NASA Astrophysics Data System (ADS)

    Hoang, M.-Q.; Boudou, L.; Le Roy, S.; Teyssedre, G.

    2014-11-01

    Thermo-stimulated depolarization current (TSDC) measurements and space charge measurements were performed on poly(ethylene naphthalene 2,6-dicarboxylate) (PEN), an aromatic and polar polyester. The aim is to develop an understanding of the dipolar and conduction processes at play in this material and in particular to understand the effects of temperature. For the TSDC measurements, when polarizing at 130 and 170 °C, the sub-glass transition and the glass transition relaxations are observed. However, in the case of a polarization temperature of 170 °C, one more current peak, labelled ρ peak, is observed at temperatures above the glass transition. This peak is not only of dipolar origin and could be associated with charge detrapping in the material. To unravel the mechanisms behind this process, a TSDC was combined with space charge measurements using the pulsed electroacoustic method (PEA) and the partial heating method was used. It is shown that the ρ peak is predominantly associated with the release of the negative charge build-up in the material.

  17. High altitude balloons with ultra thin polyethylene films for scientific observations

    NASA Astrophysics Data System (ADS)

    Nishimura, J.; Saito, Y.; Matsuzaka, Y.; Namiki, M.; Toriumi, M.; Yokota, R.; Yamagami, T.; Hirosawa, H.; Matsushima, K.

    Development of a balloon flying at higher altitude is one of the most attractive trial for the balloon technology. We, the balloon group at the Institute of Space and Astronautical Science (ISAS), have been engaged in the development since 1991. Our concept is to make a light balloon to go higher. We have developed light equipment for house keeping modules and a ultra-thin film with a thickness of only 3.4 μm. Using these equipments and the film, we launched a balloon with a volume of 30,000 m3 to reach the highest altitude of 50.8 km, which is the highest altitude ever reached by Japanese balloons. In this spring, we are going to launch a balloon with a volume of 60,000 m3 , which is expected to make a new record of the balloon altitude. We are going to report the result of the experiment.

  18. Chemical modification of poly(ethylene terephthalate) and immobilization of the selected enzymes on the modified film

    NASA Astrophysics Data System (ADS)

    Irena, Gancarz; Jolanta, Bryjak; Karolina, Zynek

    2009-07-01

    Poly(ethylene terephthalate) (PET) film was modified by reaction with hydrazine (HD), ethylenediamine (EDA), 1,2-diaminopropane (1,2-DAP) and 1,3-diaminopropane (1,3-DAP). The maximal amount of amine functionalities introduced in the chosen conditions on the surface was found as 0.07, 3.35, 0.76 and 1.99 nmol cm -2 for HD, EDA, 1,2-DAP and 1,3-DAP respectively. During the modification process etching of the sample and an increase of stiffness takes place. FTIR-ATR spectra prove that the surface chemistry after modification in amine solution is very complex. The lack of clear correlation between the surface tension and surface concentration of amine functionalities seems to confirm that. For immobilization purpose invertase, laccase and tyrosinase were used. The amount of covalently attached proteins at first increases with the increase of surface concentration of amine groups but after reaching a certain level of amine groups, decrease of the immobilization level was observed. All enzymes tested showed highest activity for a moderate level of aminolysis and this activity had the highest values for EDA-modified PET.

  19. Radiation initiated graft copolymerization of N-vinylpyrrolidone and acrylamide onto low density polyethylene films by individual and binary system

    NASA Astrophysics Data System (ADS)

    Taher, N. H.; Dessuoki, A. M.; El-Arnaouty, M. B.

    1998-10-01

    A study has been made for the preparation of membranes by the direct radiation grafting of N-vinyl pyrrolidone (NVP), acrylamide (AAm) and its comonomer onto low density polyethylene (LDPE) films. The factors affecting the grafting process such as solvent, inhibitor, radiation dose, dose rate, monomer and comonomer concentrations on the grafting yield were studied. Dioxane was chosen as a diluent and the addition of any inhibitor failed in this grafting system. The optimum comonomer composition at which the highest grafting yield was obtained, was found to be (20/80 wt% of AAm/NVP) comonomer. The dependence of the grafting rate upon NVP, AAm and its comonomer concentration for comonomer composition (50/50 and 20/80 AAm/NVP) was found to be 1.7, 1.44, 1.9 and 1.7 order, respectively. Some selective properties of the graft copolymers such as, swelling behaviour, electrical and mechanical properties were investigated. On the other hand, the thermal stability of these membranes was measured by using differential scanning calorimetry (DSC). An improvement of these properties was observed which makes possible the use of these membranes in some practical applications such as the removal of some heavy metals from waste water.

  20. Radiation-grafted polymers for biomaterial applications. I. 2-hydroxyethyl methacrylate: ethyl methacrylate grafting onto low density polyethylene films

    SciTech Connect

    Cohn, D.; Hoffman, A.S.; Ratner, B.D.

    1984-08-01

    Studies were conducted on the radiation grafting of 2-hydroxyethyl methacrylate (HEMA) and ethyl methacrylate (EMA) by the mutual irradation technique onto low density polyethylene. Four different solution concentrations were used, and radiation doses ranged from 0.03 to 0.50 Mrad. Four copolymer compositions having different HEMA:EMA ratios were also studied using two total monomer concentrations. The kinetics of the grafting process demonstrated by the two monomers were basically different. While EMA showed a typical diffusion-controlled kinetic pattern, HEMA exhibited a more complex behavior, the main features of which were an induction period, a slight autoacceleration and a significant drop in graft level after a maximum is reached. The difference in behavior was interpreted in terms of partitioning of monomers into the polyethlene substrate. The surface topography of the grafted films was studied by means of scanning electron microscopy. A mechanism based on osmotic cell formation was suggested for the HEMA graft system. The copolymer systems investigated showed that the graft reaction is faster in the initial stages for higher percentages of EMA in the monomer mixtures; as grafting proceeds the trend is reversed. 24 references, 16 figures, 2 tables.

  1. Heat shrinkability of electron-beam-modified thermoplastic elastomeric films from blends of ethylene-vinylacetate copolymer and polyethylene

    NASA Astrophysics Data System (ADS)

    Chattopadhyay, S.; Chaki, T. K.; Bhowmick, Anil K.

    2000-11-01

    The heat shrinkability of electron-beam-irradiated thermoplastic elastomeric films from blends of ethylene-vinylacetate copolymer (EVA) and low-density polyethylene (LDPE) has been investigated in this paper. The effects of temperature, time and extent of stretching and shrinkage temperature and time have been reported. Based on the above data, the optimized conditions in terms of high heat shrinkage and low amnesia rating have been evaluated. Influence of radiation doses (0-500 kGy), multifunctional sensitizer levels (ditrimethylol propane tetraacrylate, DTMPTA), and blend proportions on heat shrinkability has been explained with the help of gel fraction and X-ray data. With the increase in radiation dose, gel fraction increases, which in turn gives rise to low values of heat shrinkage and amnesia rating. At a constant radiation dose and blend ratio, percent heat shrinkage is found to decrease with increase in DTMPTA level. Gel content increases with the increase in EVA content of the blend at a constant radiation dose and monomer level, giving rise to decrease in heat shrinkability. Heat shrinkage increases with the increase in percent crystallinity, although the amnesia rating follows the reverse trend.

  2. Wetting of Functionalized Polyethylene Film Having Ionizable Organic Acids and Bases at the Polymer-Water Interface: Relations between Functional Group Polarity, Extent of Ionization, and Contact Angle with Water.

    DTIC Science & Technology

    1988-03-01

    N6) were made as for PE[>CHOH]ECH 2NH2 ]; glucosamine hydrochloride (Sigma, 2 M adjusted to pH 10 (NaOH), Film 2); glycine nydrochloride (Aldrich...Film A8, 2 11 at pH 10 (NaOH)); methylamine (Eastman, 40% in H20, Film 5; dimethylamine hydrochloride (Baker, 30% in I N NaOH, Film 6); n-octylamine

  3. Microbial Dynamics during Aerobic Exposure of Corn Silage Stored under Oxygen Barrier or Polyethylene Films▿

    PubMed Central

    Dolci, Paola; Tabacco, Ernesto; Cocolin, Luca; Borreani, Giorgio

    2011-01-01

    The aims of this study were to compare the effects of sealing forage corn with a new oxygen barrier film with those obtained by using a conventional polyethylene film. This comparison was made during both ensilage and subsequent exposure of silage to air and included chemical, microbiological, and molecular (DNA and RNA) assessments. The forage was inoculated with a mixture of Lactobacillus buchneri, Lactobacillus plantarum, and Enterococcus faecium and ensiled in polyethylene (PE) and oxygen barrier (OB) plastic bags. The oxygen permeability of the PE and OB films was 1,480 and 70 cm3 m−2 per 24 h at 23°C, respectively. The silages were sampled after 110 days of ensilage and after 2, 5, 7, 9, and 14 days of air exposure and analyzed for fermentation characteristics, conventional microbial enumeration, and bacterial and fungal community fingerprinting via PCR-denaturing gradient gel electrophoresis (DGGE) and reverse transcription (RT)-PCR-DGGE. The yeast counts in the PE and OB silages were 3.12 and 1.17 log10 CFU g−1, respectively, with corresponding aerobic stabilities of 65 and 152 h. Acetobacter pasteurianus was present at both the DNA and RNA levels in the PE silage samples after 2 days of air exposure, whereas it was found only after 7 days in the OB silages. RT-PCR-DGGE revealed the activity of Aspergillus fumigatus in the PE samples from the day 7 of air exposure, whereas it appeared only after 14 days in the OB silages. It has been shown that the use of an oxygen barrier film can ensure a longer shelf life of silage after aerobic exposure. PMID:21821764

  4. Electrical properties and surface morphology of electron beam evaporated p-type silicon thin films on polyethylene terephthalate for solar cells applications

    SciTech Connect

    Ang, P. C.; Ibrahim, K.; Pakhuruddin, M. Z.

    2015-04-24

    One way to realize low-cost thin film silicon (Si) solar cells fabrication is by depositing the films with high-deposition rate and manufacturing-compatible electron beam (e-beam) evaporation onto inexpensive foreign substrates such as glass or plastic. Most of the ongoing research is reported on e-beam evaporation of Si films on glass substrates to make polycrystalline solar cells but works combining both e-beam evaporation and plastic substrates are still scarce in the literature. This paper studies electrical properties and surface morphology of 1 µm electron beam evaporated Al-doped p-type silicon thin films on textured polyethylene terephthalate (PET) substrate for application as an absorber layer in solar cells. In this work, Si thin films with different doping concentrations (including an undoped reference) are prepared by e-beam evaporation. Energy dispersion X-ray (EDX) showed that the Si films are uniformly doped by Al dopant atoms. With increased Al/Si ratio, doping concentration increased while both resistivity and carrier mobility of the films showed opposite relationships. Root mean square (RMS) surface roughness increased. Overall, the Al-doped Si film with Al/Si ratio of 2% (doping concentration = 1.57×10{sup 16} atoms/cm{sup 3}) has been found to provide the optimum properties of a p-type absorber layer for fabrication of thin film Si solar cells on PET substrate.

  5. Radiation graft copolymerization of butyl methacrylate and acrylamide onto low density polyethylene and polypropylene films, and its application in wastewater treatment

    NASA Astrophysics Data System (ADS)

    Abdel Ghaffar, A. M.; El-Arnaouty, M. B.; Aboulfotouh, Maysara E.; Taher, N. H.; Taha, Ahmed A.

    2014-09-01

    Butyl methacrylate and acrylamide (BMA/AAm) comonomers were grafted onto low-density polyethylene (LDPE) and polypropylene (PP) films using the mutual gamma radiation grafting technique. The influences of grafting conditions such as solvent, monomer concentration, monomer composition, and irradiation dose on the grafting yield were determined. It was found that using dimethyl formamide as a solvent enhanced the copolymerization process. The grafting yield increases as the comonomer concentration increases up to 60%. Also it was found that the degree of grafting of BMA/AAm onto both LDPE and PP films increases as the AAm content increases till an optimum value at 50:50 wt%. The grafting yield of the comonomers was found to increase with increase in the radiation dose. It was observed that the degree of grafting of polyethylene films is higher than that of polypropylene (PP) films at the same conditions. Some selected properties of the graft copolymers, such as water uptake and thermal properties, were determined using thermogravimetric analysis. The morphology and structure of the grafted films were investigated using scanning electron microscopy, infra-red, and X-ray diffraction. Improvement in such properties of the prepared copolymers was observed which offers possible uses in some practical applications such as the removal of some heavy metals from wastewater. It was found that the maximum metal uptake by the copolymer followed the order Cu2+>Co2+>Ni2+ ions.

  6. Depositing radio-frequency-excited polyethylene onto the surface of microcellular polyterafluoroethylene foam film

    NASA Astrophysics Data System (ADS)

    Tang, Chongzheng; Xu, Lianxiang; Li, Chong

    1994-10-01

    Based on the physico-chemical properties of microcellular polymer foams and the mechanism of porous formation, micro and ultramicro-cellular polyteraflouroethylene porous membranes were prepared by pressure- induced phase separation in a supercritical fluid solution film. The samples were inspected by scanning electron microscope, electron spectroscopy for chemical analysis, differential scanning calorimeter and blowing bubble method. The results show that the membranes prepared by pressure-induced phase separation and then combining with plasma polymerization with ethylene, are easier to control with better characteristics.

  7. Large-scale fabrication of linear low density polyethylene/layered double hydroxides composite films with enhanced heat retention, thermal, mechanical, optical and water vapor barrier properties

    NASA Astrophysics Data System (ADS)

    Xie, Jiazhuo; Zhang, Kun; Zhao, Qinghua; Wang, Qingguo; Xu, Jing

    2016-11-01

    Novel LDH intercalated with organic aliphatic long-chain anion was large-scale synthesized innovatively by high-energy ball milling in one pot. The linear low density polyethylene (LLDPE)/layered double hydroxides (LDH) composite films with enhanced heat retention, thermal, mechanical, optical and water vapor barrier properties were fabricated by melt blending and blowing process. FT IR, XRD, SEM results show that LDH particles were dispersed uniformly in the LLDPE composite films. Particularly, LLDPE composite film with 1% LDH exhibited the optimal performance among all the composite films with a 60.36% enhancement in the water vapor barrier property and a 45.73 °C increase in the temperature of maximum mass loss rate compared with pure LLDPE film. Furthermore, the improved infrared absorbance (1180-914 cm-1) of LLDPE/LDH films revealed the significant enhancement of heat retention. Therefore, this study prompts the application of LLDPE/LDH films as agricultural films with superior heat retention.

  8. Efficacy of UV-C irradiation for inactivation of food-borne pathogens on sliced cheese packaged with different types and thicknesses of plastic films.

    PubMed

    Ha, Jae-Won; Back, Kyeong-Hwan; Kim, Yoon-Hee; Kang, Dong-Hyun

    2016-08-01

    In this study, the efficacy of using UV-C light to inactivate sliced cheese inoculated with Escherichia coli O157:H7, Salmonella Typhimurium, and Listeria monocytogenes and, packaged with 0.07 mm films of polyethylene terephthalate (PET), polyvinylchloride (PVC), polypropylene (PP), and polyethylene (PE) was investigated. The results show that compared with PET and PVC, PP and PE films showed significantly reduced levels of the three pathogens compared to inoculated but non-treated controls. Therefore, PP and PE films of different thicknesses (0.07 mm, 0.10 mm, and 0.13 mm) were then evaluated for pathogen reduction of inoculated sliced cheese samples. Compared with 0.10 and 0.13 mm, 0.07 mm thick PP and PE films did not show statistically significant reductions compared to non-packaged treated samples. Moreover, there were no statistically significant differences between the efficacy of PP and PE films. These results suggest that adjusted PP or PE film packaging in conjunction with UV-C radiation can be applied to control foodborne pathogens in the dairy industry.

  9. Optimizing fumigation efficiency by doubling drip line number and using low permeability film in raised-bed production systems

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Southern California strawberries are planted in raised-beds covered by polyethylene (PE) film and typically are irrigated with two drip lines placed near the bed surface. To control soil-borne pests, fumigants are commonly applied through the drip lines prior to transplanting strawberries, but effic...

  10. Improving fumigation efficiency by increasing drip-tape number and using low permeability film in raised-bed production systems

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Drip fumigation is commonly used for controlling soilborne pests in raised-bed strawberry production systems in California. However, the high emission loss and poor pest control indicate that the current fumigation practice with two drip tapes and polyethylene film (PE) covering need to be improved....

  11. Plasma proteins adsorption mechanism on polyethylene-grafted poly(ethylene glycol) surface by quartz crystal microbalance with dissipation.

    PubMed

    Jin, Jing; Jiang, Wei; Yin, Jinghua; Ji, Xiangling; Stagnaro, Paola

    2013-06-04

    Protein adsorption has a vital role in biomaterial surface science because it is directly related to the hemocompatibility of blood-contacting materials. In this study, monomethoxy poly(ethylene glycol) (mPEG) with two different molecular weights was grafted on polyethylene as a model to elucidate the adsorption mechanisms of plasma protein through quartz crystal microbalance with dissipation (QCM-D). Combined with data from platelet adhesion, whole blood clotting time, and hemolysis rate, the blood compatibility of PE-g-mPEG film was found to have significantly improved. Two adsorption schemes were developed for real-time monitoring of protein adsorption. Results showed that the preadsorbed bovine serum albumin (BSA) on the surfaces of PE-g-mPEG films could effectively inhibit subsequent adsorption of fibrinogen (Fib). Nonspecific protein adsorption of BSA was determined by surface coverage, not by the chain length of PEG. Dense PEG brush could release more trapped water molecules to resist BSA adsorption. Moreover, the preadsorbed Fib could be gradually displaced by high-concentration BSA. However, the adsorption and displacement of Fib was determined by surface hydrophilicity.

  12. Layer by layer assembly of a biocatalytic packaging film: lactase covalently bound to low-density polyethylene.

    PubMed

    Wong, Dana E; Talbert, Joey N; Goddard, Julie M

    2013-06-01

    Active packaging is utilized to overcome limitations of traditional processing to enhance the health, safety, economics, and shelf life of foods. Active packaging employs active components to interact with food constituents to give a desired effect. Herein we describe the development of an active package in which lactase is covalently attached to low-density polyethylene (LDPE) for in-package production of lactose-free dairy products. The specific goal of this work is to increase the total protein content loading onto LDPE using layer by layer (LbL) deposition, alternating polyethylenimine, glutaraldehyde (GL), and lactase, to enhance the overall activity of covalently attached lactase. The films were successfully oxidized via ultraviolet light, functionalized with polyethylenimine and glutaraldehyde, and layered with immobilized purified lactase. The total protein content increased with each additional layer of conjugated lactase, the 5-layer sample reaching up to 1.3 μg/cm2 . However, the increase in total protein did not lend to an increase in overall lactase activity. Calculated apparent Km indicated the affinity of immobilized lactase to substrate remains unchanged when compared to free lactase. Calculated apparent turnover numbers (kcat ) showed with each layer of attached lactase, a decrease in substrate turnover was experienced when compared to free lactase; with a decrease from 128.43 to 4.76 s(-1) for a 5-layer conjugation. Our results indicate that while LbL attachment of lactase to LDPE successfully increases total protein mass of the bulk material, the adverse impact in enzyme efficiency may limit the application of LbL immobilization chemistry for bioactive packaging use.

  13. Synergistic Effect of Atmospheric Pressure Plasma Pre-Treatment on Alkaline Etching of Polyethylene Terephthalate Fabrics and Films

    NASA Astrophysics Data System (ADS)

    A. Elabid Amel, E.; Guo, Ying; Shi, Jianjun; Ding, Ke; Zhang, Jing

    2016-04-01

    Dyeing of PET materials by traditional methods presents several problems. Plasma technology has received enormous attention as a solution for the environmental problems related with textile surface modifications, and there has been a rapid development and commercialization of plasma technology over the past decade. In this work, the synergistic effect of atmospheric pressure plasma on alkaline etching and deep coloring of dyeing properties on polyethylene terephthalate (PET) fabrics and films was investigated. The topographical changes of the PET surface were investigated by atomic force microscopy (AFM) images, which revealed a smooth surface morphology of the untreated sample whereas a high surface roughness for the plasma and/or alkaline treated samples. The effects of atmospheric pressure plasma on alkaline etching of the structure and properties of PET were investigated by means of differential scanning calorimetry (DSC), the main objective of performing DSC was to investigate the effect of the plasma pre-treatment on the Tg and Tm. Using a tensile strength tester YG065H and following a standard procedure the maximum force and elongation at maximum force of PET materials was investigated. Oxygen and argon plasma pre-treatment was found to increase the PET fabric weight loss rate. The color strength of PET fabrics was increased by various plasma pre-treatment times. The penetration of plasma and alkaline reactive species deep into the PET structure results in better dyeability and leaves a significant effect on the K/S values of the plasma pre-treated PET. It indicated that plasma pre-treatment has a great synergistic effect with the alkaline treatment of PET.

  14. Nanostructurization and thermal properties of polyethylenes' welds

    NASA Astrophysics Data System (ADS)

    Galchun, Anatoliy; Korab, Nikolay; Kondratenko, Volodymyr; Demchenko, Valeriy; Shadrin, Andriy; Anistratenko, Vitaliy; Iurzhenko, Maksym

    2015-03-01

    As it is known, polyethylene (PE) is one of the common materials in the modern world, and PE products take the major share on industrial and trade markets. For example, various types of technical PE like PE-63, PE-80, and PE-100 have wide industrial applications, i.e., in construction, for pipeline systems etc. A rapid development of plastics industry outstrips detailed investigation of welding processes and welds' formation mechanism, so they remain unexplored. There is still no final answer to the question how weld's microstructure forms. Such conditions limit our way to the understanding of the problem and, respectively, prevent scientific approaches to the welding of more complicated (from chemical point of view) types of polymers than PE. Taking into account state-of-the-art, the article presents results of complex studies of PE weld, its structure, thermophysical and operational characteristics, analysis of these results, and basing on that some hypotheses of welded joint and weld structure formation. It is shown that welding of dissimilar types of polyethylene, like PE-80 and PE-100, leads to the formation of better-ordered crystallites, restructuring the crystalline phase, and amorphous areas with internal stresses in the welding zone.

  15. Properties of polyethylene films with incorporated benzoic anhydride and/or ethyl and propyl esters of 4-hydroxybenzoic acid and their suitability for food packaging.

    PubMed

    Dobiás, J; Chudackova, K; Voldrich, M; Marek, M

    2000-12-01

    Benzoic anhydride and ethyl and propyl esters of 4-hydroxybenzoic acid (ETP and PRP, respectively, also termed parabens) incorporated into low density polyethylene (LDPE) film were studied with regard to migration into food and food simulants at 6 degrees C and 25 degrees C, and changes in selected properties of the film were investigated. Antimicrobials were incorporated into polymer film in concentrations of 5 g/kg and 10 g/kg. The addition of parabens into the polymer was more difficult than benzoic anhydride due to their volatility. For benzoic anhydride, 30-40% and 10-20% of the added amount was found to leach from the film into aqueous and olive oil food simulants, respectively. The migration into both water and olive oil followed a very similar course in the case of parabens. Migration levels over 90% and in the range of 70% to 80%, relative to the amount of agent in the film, were determined for ETP and PRP respectively. The incorporation of antimicrobials into the film significantly changed the functional characteristics of the packaging material, i.e. permeability of oxygen, carbon dioxide and water vapour, tensile strength, coefficient of friction, sealing strength and transparency. Shelf life tests with packaged cheese and toasted bread demonstrated the efficiency of the film containing 10 g/kg of BA against mould growth on the food surface during storage at 6 degrees C.

  16. Application of Linear and Branched Poly(Ethylene Glycol)-Poly(Lactide) Block Copolymers for the Preparation of Films and Solution Electrospun Meshes.

    PubMed

    Kessler, Martina; Groll, Juergen; Tessmar, Joerg

    2016-03-01

    Poly(ethylene glycol)-poly(lactide) (PEG-PLA) block copolymers are processed to solvent cast films and solution electrospun meshes. The effect of polymer composition, architecture, and number of anchoring points for the plasticizer on swelling, degradation, and mechanical properties of these films and meshes is investigated as potential barrier device for the prevention of peritoneal adhesions. As a result, adequate properties are achieved for the massive films with a longer retention of the plasticizer PEG for star-shaped block copolymers than for the linear triblock copolymers and consequently more endurable mechanical properties during degradation. For electrospun meshes fabricated using the same polymers, similar trends are observed, but with an earlier start of fragmentation and lower tensile strengths. To overcome the poor mechanical strengths and an occurring shrinkage during incubation, which may impair the coverage of the wound, further adaptions of the meshes and the fabrication process are necessary.

  17. Possibility of Solid-State Graft Copolymerization on Poly(ethylene terephthalate) Films by Plasma Irradiation and Effects of Surface Modification

    NASA Astrophysics Data System (ADS)

    Narushima, Kazuo; Matsuda, Noriko; Mizutani, Chie; Yamashita, Nanami; Inagaki, Norihiro; Iio, Kokoro; Isono, Yoshihiro; Islam, Mohammed Rafiqul

    2007-07-01

    A solid-state graft copolymerization for poly(ethylene terephthalate) (PET) films was proposed for a new surface modification technique. The functional groups included in graft monomers can be introduced on a PET surface. Allylbiguanide hydrochloric acid salt (ABG), N-methylol acrylamide (NM-AAm), and N-isopropyl acrylamide (NIP-AAm) were used as graft monomers. This technique led to a large change in the N/C atomic ratio on the PET film surfaces, which shows that nitrogen functional groups were introduced on PET surfaces. On the grafted PET films, a new N 1s spectrum appeared. This N 1s spectrum contained two components, namely, amino and amido groups, which suggests that the two groups were introduced onto the PET surfaces. In particular, isopropyl groups were introduced on the PET surface in the case of NIP-AAm. The formation of these functional groups demonstrated changes in the surface properties of PET, such as improved wettability.

  18. Fabrication of nanopatterned poly(ethylene glycol) brushes by molecular transfer printing from poly(styrene-block-methyl methacrylate) films to generate arrays of Au nanoparticles.

    PubMed

    Onses, M Serdar

    2015-01-27

    This article presents a soft lithographic approach using block copolymer (BCP) films to fabricate functional chemically patterned polymer brushes on the nanoscale. Hydroxyl-terminated poly(ethylene glycol) (PEG-OH) was transfer printed from the poly(methyl methacrylate) (PMMA) domains of self-assembled poly(styrene-block-methyl methacrylate) films to a substrate in conformal contact with the film to generate patterned PEG brushes mirroring the pattern of BCP domains. A key point in the study is that the chemistry of the functional transferred brushes is different from the chemistry of either block of the copolymer; PEG-OH is miscible only in the PMMA block and therefore transferred only from PMMA domains. The functionality of the PEG brushes was demonstrated by the selective immobilization of citrate-stabilized Au NPs (15 nm) and validated the generation of high-quality chemical patterns with sub-30-nm feature sizes.

  19. Characterization of Polyethylene-Graft-Sulfonated Polyarylsulfone Proton Exchange Membranes for Direct Methanol Fuel Cell Applications.

    PubMed

    Kim, Hyung Kyu; Zhang, Gang; Nam, Changwoo; Chung, T C Mike

    2015-12-04

    This paper examines polymer film morphology and several important properties of polyethylene-graft-sulfonated polyarylene ether sulfone (PE-g-s-PAES) proton exchange membranes (PEMs) for direct methanol fuel cell applications. Due to the extreme surface energy differences between a semi-crystalline and hydrophobic PE backbone and several amorphous and hydrophilic s-PAES side chains, the PE-g-s-PAES membrane self-assembles into a unique morphology, with many proton conductive s-PAES channels embedded in the stable and tough PE matrix and a thin hydrophobic PE layer spontaneously formed on the membrane surfaces. In the bulk, these membranes show good mechanical properties (tensile strength >30 MPa, Young's modulus >1400 MPa) and low water swelling (λ < 15) even with high IEC >3 mmol/g in the s-PAES domains. On the surface, the thin hydrophobic and semi-crystalline PE layer shows some unusual barrier (protective) properties. In addition to exhibiting higher through-plane conductivity (up to 160 mS/cm) than in-plane conductivity, the PE surface layer minimizes methanol cross-over from anode to cathode with reduced fuel loss, and stops the HO• and HO₂• radicals, originally formed at the anode, entering into PEM matrix. Evidently, the thin PE surface layer provides a highly desirable protecting layer for PEMs to reduce fuel loss and increase chemical stability. Overall, the newly developed PE-g-s-PAES membranes offer a desirable set of PEM properties, including conductivity, selectivity, mechanical strength, stability, and cost-effectiveness for direct methanol fuel cell applications.

  20. Characterization of Polyethylene-Graft-Sulfonated Polyarylsulfone Proton Exchange Membranes for Direct Methanol Fuel Cell Applications

    PubMed Central

    Kim, Hyung Kyu; Zhang, Gang; Nam, Changwoo; Chung, T.C. Mike

    2015-01-01

    This paper examines polymer film morphology and several important properties of polyethylene-graft-sulfonated polyarylene ether sulfone (PE-g-s-PAES) proton exchange membranes (PEMs) for direct methanol fuel cell applications. Due to the extreme surface energy differences between a semi-crystalline and hydrophobic PE backbone and several amorphous and hydrophilic s-PAES side chains, the PE-g-s-PAES membrane self-assembles into a unique morphology, with many proton conductive s-PAES channels embedded in the stable and tough PE matrix and a thin hydrophobic PE layer spontaneously formed on the membrane surfaces. In the bulk, these membranes show good mechanical properties (tensile strength >30 MPa, Young’s modulus >1400 MPa) and low water swelling (λ < 15) even with high IEC >3 mmol/g in the s-PAES domains. On the surface, the thin hydrophobic and semi-crystalline PE layer shows some unusual barrier (protective) properties. In addition to exhibiting higher through-plane conductivity (up to 160 mS/cm) than in-plane conductivity, the PE surface layer minimizes methanol cross-over from anode to cathode with reduced fuel loss, and stops the HO• and HO2• radicals, originally formed at the anode, entering into PEM matrix. Evidently, the thin PE surface layer provides a highly desirable protecting layer for PEMs to reduce fuel loss and increase chemical stability. Overall, the newly developed PE-g-s-PAES membranes offer a desirable set of PEM properties, including conductivity, selectivity, mechanical strength, stability, and cost-effectiveness for direct methanol fuel cell applications. PMID:26690232

  1. Mechanical and transparent conductive properties of ZnO and Ga-doped ZnO films sputtered using electron-cyclotron-resonance plasma on polyethylene naphtalate substrates

    SciTech Connect

    Akazawa, Housei

    2014-03-15

    Transparent conductive ZnO and Ga-doped ZnO (GZO) films were deposited on polyethylene naphtalate (PEN) sheet substrates using electron cyclotron resonance plasma sputtering. Both ZnO and GZO films were highly adhesive to the PEN substrates without inserting an intermediate layer in the interface. When compared at the same thickness, the transparent conductive properties of GZO films on PEN substrates were only slightly inferior to those on glass substrates. However, the carrier concentration of ZnO films on PEN substrates was 1.5 times that of those on glass substrates, whereas their Hall mobility was only 60% at a thickness of 300 nm. The depth profile of elements measured by secondary ion mass spectroscopy revealed the diffusion of hydrocarbons out of the PEN substrate into the ZnO film. Hence, doped carbons may act as donors to enhance carrier concentration, and the intermixing of elements at the interface may deteriorate the crystallinity, resulting in the lower Hall mobility. When the ZnO films were thicker than 400 nm, cracks became prevalent because of the lattice mismatch strain between the film and the substrate, whereas GZO films were free of cracks. The authors investigated how rolling the films around a cylindrical pipe surface affected their conductive properties. Degraded conductivity occurred at a threshold pipe radius of 10 mm when tensile stress was applied to the film, but it occurred at a pipe radius of 5 mm when compressive stress was applied. These values are guidelines for bending actual devices fabricated on PEN substrates.

  2. Suppression of cell and platelet adhesion to star-shaped 8-armed poly(ethylene glycol)-poly(L-lactide) block copolymer films.

    PubMed

    Nagahama, Koji; Ohya, Yuichi; Ouchi, Tatsuro

    2006-06-16

    To explore the potential of a star-shaped 8-armed poly(ethylene glycol)35K-block-poly(L-lactide)37K (8-armed PEG35K-b-PLLA37K: M(n) of PEG = 35 000, M(n) of PLLA = 37 000) film as a novel bioabsorbable adhesion-prevention membrane, the water structure, surface contact angle, protein adsorption, and cell and platelet anti-adhesion properties of such a hydrated film are investigated. Based on the results, it is found that the 8-armed PEG35K-b-PLLA37K film exhibits a biologically inert surface, which is the result of a large number of PEG chains and a free water layer on the film surface. This leads to a reduction in protein absorption and cell and platelet adhesion onto the film surface. This implies that the star-shaped 8-armed PEG35K-b-PLLA37K film can be utilized as a novel bioabsorbable adhesion-prevention membrane.

  3. Spontaneous and specific myogenic differentiation of human mesenchymal stem cells on polyethylene glycol-linked multi-walled carbon nanotube films for skeletal muscle engineering.

    PubMed

    Zhao, Chunyan; Andersen, Henrik; Ozyilmaz, Barbaros; Ramaprabhu, Sundara; Pastorin, Giorgia; Ho, Han Kiat

    2015-11-21

    This study explored the influence of polyethylene glycol-linked multi-walled carbon nanotube (PEG-CNT) films on skeletal myogenic differentiation of human mesenchymal stem cells (hMSCs). PEG-CNT films were prepared with nanoscale surface roughness, orderly arrangement of PEG-CNTs, high hydrophilicity and high mechanical strength. Notably, PEG-CNT films alone could direct the skeletal myogenic differentiation of hMSCs in the absence of myogenic induction factors. The quantitative real-time polymerase chain reaction (RT-PCR) showed that the non-induced hMSCs plated on the PEG-CNT films, compared to the negative control, presented significant up-regulation of general myogenic markers including early commitment markers of myoblast differentiation protein-1 (MyoD) and desmin, as well as a late phase marker of myosin heavy chain-2 (MHC). Corresponding protein analysis by immunoblot assays corroborated these results. Skeletal muscle-specific markers, fast skeletal troponin-C (TnC) and ryanodine receptor-1 (Ryr) were also significantly increased in the non-induced hMSCs on PEG-CNT films by RT-PCR. For these cells, the commitment to specific skeletal myoblasts was further proved by the absence of enhanced adipogenic, chondrogenic and osteogenic markers. This study elucidated that PEG-CNT films supported a dedicated differentiation of hMSCs into a skeletal myogenic lineage and can work as a promising material towards skeletal muscle injury repair.

  4. Thermal, mechanical and permeation properties of gamma-irradiated multilayer food packaging films containing a buried layer of recycled low-density polyethylene

    NASA Astrophysics Data System (ADS)

    Chytiri, Stavroula; Goulas, Antonios E.; Riganakos, Kyriakos A.; Kontominas, Michael G.

    2006-03-01

    The effect of gamma radiation (doses 5-60 kGy) on the thermal, mechanical and permeation properties, as well as on IR-spectra of experimental five-layer food packaging films were studied. Films contained a middle buried layer of recycled low-density polyethylene (LDPE) comprising 25-50% by weight of the multilayer structure. Representative films containing 100% virgin LDPE as the buried layer were taken as controls. Results showed that the percentage of recycled LDPE in the multilayer structure did not significantly ( p<0.05) affect the melting temperature, tensile strength, percent elongation at break, Young's modulus, oxygen, carbon dioxide and water vapour transmission rate values and the IR-spectra of the non-irradiated and irradiated multilayer films. Irradiation (mainly the higher dose of 60 kGy) induced certain small, but statistically significant ( p<0.05) differences in the mechanical properties of multilayer films (with or without recycled LDPE layer) while no significant differences were observed in the thermal properties and in the gas and water vapour permeability of multilayer films. The above findings are discussed in relation to the good quality of the pre-consumer scrap used in the present study.

  5. Effect of peptide secondary structure on adsorption and adsorbed film properties on end-grafted polyethylene oxide layers.

    PubMed

    Binazadeh, M; Zeng, H; Unsworth, L D

    2014-01-01

    Poly-l-lysine (PLL), in α-helix or β-sheet configuration, was used as a model peptide for investigating the effect of secondary structures on adsorption events to poly(ethylene oxide) (PEO) modified surfaces formed using θ solvents. Circular dichroism results showed that the secondary structure of PLL persisted upon adsorption to Au and PEO modified Au surfaces. Quartz crystal microbalance with dissipation (QCM-D) was used to characterize the chemisorbed PEO layer in different solvents (θ and good solvents), as well as the sequential adsorption of PLL in different secondary structures (α-helix or β-sheet). QCM-D results suggest that chemisorption of PEO 750 and 2000 from θ solutions led to brushes 3.8 ± 0.1 and 4.5 ± 0.1 nm thick with layer viscosities of 9.2 ± 0.8 and 4.8 ± 0.5 cP, respectively. The average number of H2O per ethylene oxides, while in θ solvent, was determined as ~0.9 and ~1.2 for the PEO 750 and 2000 layers, respectively. Upon immersion in good solvent (as used for PLL adsorption experiments), the number of H2O per ethylene oxides increased to ~1.5 and ~2.0 for PEO 750 and 2000 films, respectively. PLL adsorbed masses for α-helix and β-sheet on Au sensors was 231 ± 5 and 1087 ± 14 ng cm(-2), with layer viscosities of 2.3 ± 0.1 and 1.2 ± 0.1 cP, respectively; suggesting that the α-helix layer was more rigid, despite a smaller adsorbed mass, than that of β-sheet layers. The PEO 750 layer reduced PLL adsorbed amounts to ~10 and 12% of that on Au for α-helices and β-sheets respectively. The PLL adsorbed mass to PEO 2000 layers dropped to ~12% and 4% of that on Au, for α-helix and β-sheet respectively. No significant differences existed for the viscosities of adsorbed α-helix and β-sheet PLL on PEO surfaces. These results provide new insights into the fundamental understanding of the effects of secondary structures of peptides and proteins on their surface adsorption.

  6. Poly(methyl methacrylate-co-ethyl acrylate) latex particles with poly(ethylene glycol) grafts: structure and film formation.

    PubMed

    Schantz, Staffan; Carlsson, Hans T; Andersson, Thomas; Erkselius, Stefan; Larsson, Anders; Karlsson, Ola J

    2007-03-27

    Water-based copolymer dispersions were prepared using methyl methacrylate (MMA), ethyl acrylate (EA) (MMA/EA = 1:2), and a series of nonionic polymerizable surfactants, i.e., "surfmers" based on poly(ethylene glycol)-(meth)acrylates. The latexes were compared with the behavior of a conventionally stabilized (nonionic nonylphenol ethoxylate, NP100 with 84 ethylene oxide units) dispersion with the same MMA-EA composition (PMMAEA). A number of techniques were employed in order to characterize structure, dynamics, and film formation properties: solution/solid-state NMR, dynamic/static light scattering (DLS/SLS), differential scanning calorimetry (DSC), tensile/shear mode dynamic mechanical thermal analysis (DMTA), and atomic force microscopy (AFM). The surfmers were found to be miscible with the MMA-EA copolymer at room temperature, with 46-85 mol % of the reacted surfmer detected at the particle surfaces, and the remaining part buried in the particle bulk. In contrast, the NP100 surfactant formed a separate interphase between the copolymer particles with no mixing detected at room temperature or at 90 degrees C. For a 4.0% dry weight concentration, NP100 phase separated and further crystallized at room temperature over a period of several months. Composition fluctuations related to a limited blockiness on a length scale above approximately 2 nm were detected for PMMAEA particles, whereas the surfmer particles were found to be homogeneous also below this limit. On a particle-particle level, the dispersions tended to form colloidal crystals unless hindered by a broadened particle size distribution or, in the case of PMMAEA, by the action of NP100. Finally, a surface roughness (Rq) master plot was constructed for data above the glass transition temperature (Tg) from Tg + 11 degrees C to Tg + 57 degrees C and compared with the complex shear modulus over 11 frequency decades. Shift factors from the 2 methods obeyed the same Williams-Landel-Ferry (WLF) temperature

  7. Effects of Interphase Modification and Biaxial Orientation on Dielectric Properties of Poly(ethylene terephthalate)/Poly(vinylidene fluoride-co-hexafluoropropylene) Multilayer Films.

    PubMed

    Yin, Kezhen; Zhou, Zheng; Schuele, Donald E; Wolak, Mason; Zhu, Lei; Baer, Eric

    2016-06-01

    Recently, poly(vinylidene fluoride) (PVDF)-based multilayer films have demonstrated enhanced dielectric properties, combining high energy density and high dielectric breakdown strength from the component polymers. In this work, further enhanced dielectric properties were achieved through interface/interphase modulation and biaxial orientation for the poly(ethylene terephthalate)/poly(methyl methacrylate)/poly(vinylidene fluoride-co-hexafluoropropylene) [PET/PMMA/P(VDF-HFP)] three-component multilayer films. Because PMMA is miscible with P(VDF-HFP) and compatible with PET, the interfacial adhesion between PET and P(VDF-HFP) layers should be improved. Biaxial stretching of the as-extruded multilayer films induced formation of highly oriented fibrillar crystals in both P(VDF-HFP) and PET, resulting in improved dielectric properties with respect to the unstretched films. First, the parallel orientation of PVDF crystals reduced the dielectric loss from the αc relaxation in α crystals. Second, biaxial stretching constrained the amorphous phase in P(VDF-HFP) and thus the migrational loss from impurity ions was reduced. Third, biaxial stretching induced a significant amount of rigid amorphous phase in PET, further enhancing the breakdown strength of multilayer films. Due to the synergistic effects of improved interfacial adhesion and biaxial orientation, the PET/PMMA/P(VDF-HFP) 65-layer films with 8 vol % PMMA exhibited optimal dielectric properties with an energy density of 17.4 J/cm(3) at breakdown and the lowest dielectric loss. These three-component multilayer films are promising for future high-energy-density film capacitor applications.

  8. Morphological and Chemical Evolution of Gradually Deposited Diamond-Like Carbon Films on Polyethylene Terephthalate: From Subplantation Processes to Structural Reorganization by Intrinsic Stress Release Phenomena.

    PubMed

    Catena, Alberto; Guo, Qiaochu; Kunze, Michael R; Agnello, Simonpietro; Gelardi, Franco M; Wehner, Stefan; Fischer, Christian B

    2016-04-27

    Diamond-like carbon (DLC) films on polyethylene terephthalate (PET) are nowadays intensively studied composites due to their excellent gas barrier properties and biocompatibility. Despite their applicative features being highly explored, the interface properties and structural film evolution of DLC coatings on PET during deposition processes are still sparsely investigated. In this study two different types of DLC films were gradually deposited on PET by radio frequency plasma-enhanced chemical vapor deposition (RF-PECVD) using acetylene plasma. The surface morphology of the deposited samples has been analyzed by atomic force microscopy (AFM). Their chemical composition was investigated by diffusive reflectance infrared Fourier transform (DRIFT) and Raman spectroscopy analysis and the surface wettability by contact angle measurements. Subplantation processes and interface effects are revealed through the morphological and chemical analysis of both types. During plasma deposition processes the increasing carbon load causes the rise of intrinsic film stress. It is proven that stress release phenomena cause the transition between polymer-like to a more cross-linked DLC network by folding dehydrogenated chains into closed 6-fold rings. These findings significantly lead to an enhanced understanding in DLC film growth mechanism by RF-PECVD processes.

  9. Application of sample-sample two-dimensional correlation spectroscopy to determine the glass transition temperature of poly(ethylene terephthalate) thin films.

    PubMed

    Hu, Yun; Zhang, Ying; Li, Boyan; Ozaki, Yukihiro

    2007-01-01

    The glass transition temperatures (Tg) of poly(ethylene terephthalate) (PET) thin films with different thicknesses are determined by analyzing their in situ reflection-absorption infrared (RAIR) spectra measured over a temperature range of 28 to 84 degrees C. The criterion of standard deviation of the covariance matrices is used as a graphical indicator for the determination of the Tg present in the sample-sample two-dimensional (2D) correlation spectra calculated from the temperature-dependent RAIR spectra. After two data pretreatments of the first derivative of the spectral absorbance versus temperature and the mean normalization over the wavenumbers are sequentially carried out on the RAIR spectra, an abrupt change of the first-derivative correlation spectra with respect to temperature is quickly obtained. It reflects the temperature at which the apparent intensity changes in pertinent absorption bands of PET thin films take place due to the dramatic segmental motion of PET chain conformation. The Tg of the thin PET films is accordingly determined. The results reveal that it decreases with a great dependence on the film thickness and that sample-sample 2D correlation spectroscopy enables one to determine the transition temperature of polymer thin films in an easy and valid way.

  10. Polyethylene Oxide Films Polymerized by Radio Frequency Plasma-Enhanced Chemical Vapour Phase Deposition and Its Adsorption Behaviour of Platelet-Rich Plasma

    NASA Astrophysics Data System (ADS)

    Hu, Wen-Juan; Xie, Fen-Yan; Chen, Qiang; Weng, Jing

    2008-10-01

    We present polyethylene oxide (PEO) functional films polymerized by rf plasma-enhanced vapour chemical deposition (rf-PECVD) on p-Si (100) surface with precursor ethylene glycol dimethyl ether (EGDME) and diluted Ar in pulsed plasma mode. The influences of discharge parameters on the film properties and compounds are investigated. The film structure is analysed by Fourier transform infrared (FTIR) spectroscopy. The water contact angle measurement and atomic force microscope (AFM) are employed to examine the surface polarity and to detect surface morphology, respectively. It is concluded that the smaller duty cycle in pulsed plasma mode contributes to the rich C-O-C (EO) group on the surfaces. As an application, the adsorption behaviour of platelet-rich plasma on plasma polymerization films performed in-vitro is explored. The shapes of attached cells are studied in detail by an optic invert microscope, which clarifies that high-density C-O-C groups on surfaces are responsible for non-fouling adsorption behaviour of the PEO films.

  11. Surface Functionalized Polyethylene Film.

    DTIC Science & Technology

    1986-06-01

    functionality into this oxidized surface layer. 2) Explored new techniques for analyzing the surfaces of organic polymeric solids. Contact angle titration...the study of the contact angle of water on organic solids as a function of pH--has proved particularly useful and extremely surface sensitive. 3

  12. Comparison of Mechanical Properties Between PE80 and PE100 Pipe Materials

    NASA Astrophysics Data System (ADS)

    Zhang, Yi; Jar, P.-Y. Ben

    2016-10-01

    Mechanical properties, including yield stress, relaxation behavior, moduli (elastic modulus at the strain of 0.5% and strain hardening modulus at strains above 70%), viscous stress, and quasi-static stress, are compared between polyethylene (PE) pipes that are made of PE80 and PE100 resins. The mechanical properties are measured using D-split tensile test on modified notched pipe ring specimens. The comparison includes the influence of strain rate (by the change of crosshead speed) on the yield strength and influence of pre-strain on the relaxation behavior and the modulus values. A two-stage approach is used to characterize the influence of pre-strain on the moduli, to ensure that viscous recovery from the first-stage of the test, to introduce the pre-strain, does not affect the modulus measurement from the second-stage test. The results show that elastic modulus, yield stress, strain hardening modulus, viscous stress, and quasi-static stress for PE100 are higher than those for PE80, but PE80 shows higher resistance to stress relaxation. The results also show that with the increase in the pre-strain level, the elastic modulus drops but the strain hardening modulus remains relatively constant.

  13. Multivariate analysis of DSC-XRD simultaneous measurement data: a study of multistage crystalline structure changes in a linear poly(ethylene imine) thin film.

    PubMed

    Kakuda, Hiroyuki; Okada, Tetsuo; Otsuka, Makoto; Katsumoto, Yukiteru; Hasegawa, Takeshi

    2009-01-01

    A multivariate analytical technique has been applied to the analysis of simultaneous measurement data from differential scanning calorimetry (DSC) and X-ray diffraction (XRD) in order to study thermal changes in crystalline structure of a linear poly(ethylene imine) (LPEI) film. A large number of XRD patterns generated from the simultaneous measurements were subjected to an augmented alternative least-squares (ALS) regression analysis, and the XRD patterns were readily decomposed into chemically independent XRD patterns and their thermal profiles were also obtained at the same time. The decomposed XRD patterns and the profiles were useful in discussing the minute peaks in the DSC. The analytical results revealed the following changes of polymorphisms in detail: An LPEI film prepared by casting an aqueous solution was composed of sesquihydrate and hemihydrate crystals. The sesquihydrate one was lost at an early stage of heating, and the film changed into an amorphous state. Once the sesquihydrate was lost by heating, it was not recovered even when it was cooled back to room temperature. When the sample was heated again, structural changes were found between the hemihydrate and the amorphous components. In this manner, the simultaneous DSC-XRD measurements combined with ALS analysis proved to be powerful for obtaining a better understanding of the thermally induced changes of the crystalline structure in a polymer film.

  14. Radiolysis products and sensory properties of electron-beam-irradiated high-barrier food-packaging films containing a buried layer of recycled low-density polyethylene.

    PubMed

    Chytiri, S D; Badeka, A V; Riganakos, K A; Kontominas, M G

    2010-04-01

    The aim was to study the effect of electron-beam irradiation on the production of radiolysis products and sensory changes in experimental high-barrier packaging films composed of polyamide (PA), ethylene-vinyl alcohol (EVOH) and low-density polyethylene (LDPE). Films contained a middle buried layer of recycled LDPE, while films containing 100% virgin LDPE as the middle buried layer were taken as controls. Irradiation doses ranged between zero and 60 kGy. Generally, a large number of radiolysis products were produced during electron-beam irradiation, even at the lower absorbed doses of 5 and 10 kGy (approved doses for food 'cold pasteurization'). The quantity of radiolysis products increased with irradiation dose. There were no significant differences in radiolysis products identified between samples containing a recycled layer of LDPE and those containing virgin LDPE (all absorbed doses), indicating the 'functional barrier' properties of external virgin polymer layers. Sensory properties (mainly taste) of potable water were affected after contact with irradiated as low as 5 kGy packaging films. This effect increased with increasing irradiation dose.

  15. Structural and optical properties of Ag-doped copper oxide thin films on polyethylene napthalate substrate prepared by low temperature microwave annealing

    SciTech Connect

    Das, Sayantan; Alford, T. L.

    2013-06-28

    Silver doped cupric oxide thin films are prepared on polyethylene naphthalate (flexible polymer) substrates. Thin films Ag-doped CuO are deposited on the substrate by co-sputtering followed by microwave assisted oxidation of the metal films. The low temperature tolerance of the polymer substrates led to the search for innovative low temperature processing techniques. Cupric oxide is a p-type semiconductor with an indirect band gap and is used as selective absorption layer solar cells. X-ray diffraction identifies the CuO phases. Rutherford backscattering spectrometry measurements confirm the stoichiometry of each copper oxide formed. The surface morphology is determined by atomic force microscopy. The microstructural properties such as crystallite size and the microstrain for (-111) and (111) planes are calculated and discussed. Incorporation of Ag led to the lowering of band gap in CuO. Consequently, it is determined that Ag addition has a strong effect on the structural, morphological, surface, and optical properties of CuO grown on flexible substrates by microwave annealing. Tauc's plot is used to determine the optical band gap of CuO and Ag doped CuO films. The values of the indirect and direct band gap for CuO are found to be 2.02 eV and 3.19 eV, respectively.

  16. Roll-to-roll DBD plasma pretreated polyethylene web for enhancement of Al coating adhesion and barrier property

    NASA Astrophysics Data System (ADS)

    Zhang, Haibao; Li, Hua; Fang, Ming; Wang, Zhengduo; Sang, Lijun; Yang, Lizhen; Chen, Qiang

    2016-12-01

    In this paper the roll-to-roll atmospheric dielectric barrier discharge (DBD) was used to pre-treat polyethylene (PE) web surface before the conventional thermal evaporation aluminum (Al) was performed as a barrier layer. We emphasized the plasma environment effect based on the inlet three kinds of reactive monomers. The cross hatch test was employed to assess the Al coating adhesion; and the oxygen transmission rate (OTR) was used to evaluate gas barrier property. The results showed that after roll-to-roll DBD plasma treatment all Al coatings adhered strongly on PE films and were free from pinhole defects with mirror morphology. The OTR was reduced from 2673 cm3/m2 day for Al-coated original PE to 138 cm3/m2 day for Al-coated allyamine (C3H7N) modified PE. To well understand the mechanism the chemical compositions of the untreated and DBD plasma pretreated PE films were analyzed by X-ray photoelectron spectroscopy (XPS). The surface topography was characterized by atomic force microscopy (AFM). For the property of surface energy the water contact angle measurement was also carried out in the DBD plasma treated samples with deionized water.

  17. Spontaneous and specific myogenic differentiation of human mesenchymal stem cells on polyethylene glycol-linked multi-walled carbon nanotube films for skeletal muscle engineering

    NASA Astrophysics Data System (ADS)

    Zhao, Chunyan; Andersen, Henrik; Ozyilmaz, Barbaros; Ramaprabhu, Sundara; Pastorin, Giorgia; Ho, Han Kiat

    2015-10-01

    This study explored the influence of polyethylene glycol-linked multi-walled carbon nanotube (PEG-CNT) films on skeletal myogenic differentiation of human mesenchymal stem cells (hMSCs). PEG-CNT films were prepared with nanoscale surface roughness, orderly arrangement of PEG-CNTs, high hydrophilicity and high mechanical strength. Notably, PEG-CNT films alone could direct the skeletal myogenic differentiation of hMSCs in the absence of myogenic induction factors. The quantitative real-time polymerase chain reaction (RT-PCR) showed that the non-induced hMSCs plated on the PEG-CNT films, compared to the negative control, presented significant up-regulation of general myogenic markers including early commitment markers of myoblast differentiation protein-1 (MyoD) and desmin, as well as a late phase marker of myosin heavy chain-2 (MHC). Corresponding protein analysis by immunoblot assays corroborated these results. Skeletal muscle-specific markers, fast skeletal troponin-C (TnC) and ryanodine receptor-1 (Ryr) were also significantly increased in the non-induced hMSCs on PEG-CNT films by RT-PCR. For these cells, the commitment to specific skeletal myoblasts was further proved by the absence of enhanced adipogenic, chondrogenic and osteogenic markers. This study elucidated that PEG-CNT films supported a dedicated differentiation of hMSCs into a skeletal myogenic lineage and can work as a promising material towards skeletal muscle injury repair.This study explored the influence of polyethylene glycol-linked multi-walled carbon nanotube (PEG-CNT) films on skeletal myogenic differentiation of human mesenchymal stem cells (hMSCs). PEG-CNT films were prepared with nanoscale surface roughness, orderly arrangement of PEG-CNTs, high hydrophilicity and high mechanical strength. Notably, PEG-CNT films alone could direct the skeletal myogenic differentiation of hMSCs in the absence of myogenic induction factors. The quantitative real-time polymerase chain reaction (RT-PCR) showed

  18. Fluorescence Properties of Dansyl Groups Covalently Bonded to the Surface of Oxidatively Functionalized Low-Density Polyethylene Film.

    DTIC Science & Technology

    1985-12-01

    the nature of the group linking the Dansyl moiety to the surface, and to change the structures and properties of other organic groups present on the...they are undoubtedly less important than reactions involving acid chloride moieties, and that, in any event, the nature of the group linking the...increasing pH as the amino group is deprotonated. We conclude that the nature of the surface groups on PE-D

  19. Phenolic content and antioxidant activity of olive by-products and antioxidant film containing olive leaf extract.

    PubMed

    Moudache, M; Colon, M; Nerín, C; Zaidi, F

    2016-12-01

    The antioxidant activity of olive leaf (OL) and cake (OC) extracts with different solvents was evaluated. 70% of aqueous ethanol extract of OL was chosen as the most antioxidant extract based on antiradical activity (DPPH) (95.4±0.3%) and oxygen radical absorbance capacity (ORAC) (0.82±0.07g equivalent Trolox per g of solution) assays. This OL extract was incorporated in two multilayer materials consisting of (i) polyethylene/polyethylene (PE/PE) film and (ii) polyethylene/paper (PE/P). These multilayers were exposed to a gas stream enriched in free radicals to evaluate the scavenging capacity of both materials. PE/PE film exhibited the highest scavenging activity of free radicals (78.8%). Migration of the phenolic compounds from olive by-products into two simulants was performed and demonstrated a non-migrating behavior. The limits of detection and quantification for oleuropein were 0.5μgkg(-1) and 1.7μgkg(-1) and for Luteolin-7-O-glucoside 1.3μgkg(-1) and 4.3μg kg(-1) respectively.

  20. Plasma-induced graft-polymerization of polyethylene glycol acrylate on polypropylene films: chemical characterization and evaluation of the protein adsorption.

    PubMed

    Zanini, Stefano; Riccardi, Claudia; Grimoldi, Elisa; Colombo, Claudia; Villa, Anna Maria; Natalello, Antonino; Gatti-Lafranconi, Pietro; Lotti, Marina; Doglia, Silvia Maria

    2010-01-01

    This work deals with the optimization of argon plasma-induced graft-polymerization of polyethylene glycol acrylate (PEGA) on polypropylene (PP) films in order to obtain surfaces with a reduced protein adsorption for possible biomedical applications. To this end, we examined the protein adsorption on the treated and untreated surfaces. The graft-polymerization process consisted of four steps: (a) plasma pre-activation of the PP substrates; (b) immersion in a PEGA solution; (c) argon plasma-induced graft-polymerization; (d) washing and drying of the samples. The efficiency of these processes was evaluated in terms of the amount of grafted polymer, coverage uniformity and substrates wettability. The process was monitored by contact angle measurements, attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR), X-ray Photoelectron Spectroscopy (XPS) and atomic force microscopy (AFM) analyses. The stability of the obtained thin films was evaluated in water and in Phosphate Buffer Saline (PBS) at 37 degrees C. The adsorption of fibrinogen and green fluorescent protein (GFP)--taken as model proteins--on the differently prepared surfaces was evaluated through a fluorescence approach using laser scanning confocal microscopy with photon counting detection. After plasma treatments of short duration, the protein adsorption decreases by about 60-70% with respect to that of the untreated film, while long plasma exposure resulted in a higher protein adsorption, due to damaging of the grafted polymer.

  1. Radiation induced graft copolymerization of n-butyl acrylate onto poly(ethylene terephthalate) (PET) films and thermal properties of the obtained graft copolymer

    NASA Astrophysics Data System (ADS)

    Ping, Xiang; Wang, Mozhen; Ge, Xuewu

    2011-05-01

    n-Butyl acrylate (BA) was successfully grafted onto poly(ethylene terephthalate) (PET) film using simultaneous radiation induced graft copolymerization with gamma rays. When BA concentration ranges from 20% to 30%, the Degree of Grafting (DG), measured by gravimetry and 1H NMR, increases with the monomer concentration and absorbed dose, but decreases with dose rate from 0.83 to 2.53 kGy/h. The maximum DG can reach up to 22.1%. The thermal transition temperatures such as glass-transition temperature ( Tg) and cold-crystallization temperature ( Tcc) of PET in grafted films were little different from those in original PET film, indicating that microphase separation occurred between PBA side chains and PET backbone. This work implied that if PET/elastomers (e.g., acrylate rubber) blends are radiated by high energy gamma rays under a certain condition, PET-g-polyacrylate copolymer may be produced in-situ, which will improve the compatibility between PET and the elastomers so as to improve the integral mechanical properties of PET based engineering plastic.

  2. Silk fibroin immobilization on poly(ethylene terephthalate) films: comparison of two surface modification methods and their effect on mesenchymal stem cells culture.

    PubMed

    Liang, Meini; Yao, Jinrong; Chen, Xin; Huang, Lei; Shao, Zhengzhong

    2013-04-01

    Silk fibroin (SF) has played a curial role for the surface modification of conventional materials to improve the biocompatibility, and SF modified poly(ethylene terephthalate) (PET) materials have potential applications on tissue engineering such as artificial ligament, artificial vessel, artificial heart valve sewing cuffs dacron and surgical mesh engineering. In this work, SF was immobilized onto PET film via two different methods: 1) plasma pretreatment followed by SF dip coating (PET-SF) and 2) plasma-induce acrylic acid graft polymerization and subsequent covalent immobilization of SF on PET film (PET-PAA-SF). It could be found that plasma treatment provided higher surface roughness which was suitable for further SF dip coating, while grafted poly(acrylic acid) (PAA) promised the covalent bonding between SF and PAA. ATR-FTIR adsorption band at 3284 cm(-1), 1623 cm(-1) and 1520 cm(-1) suggested the successful introduction of SF onto PET surface, while the amount of immobilized SF of PET-SF was higher than PET-PAA-SF according to XPS investigation (0.29 vs 0.23 for N/C ratio). Surface modified PET film was used as substrate for mesenchymal stem cells (MSCs) culture, the cells on PET-SF surface exhibited optimum density compared to PET-PAA-SF according to CCK-8 assays, which indicated that plasma pretreatment followed by SF dip coating was a simple and effective way to prepare biocompatible PET surface.

  3. Tuning the superstructure of ultrahigh-molecular-weight polyethylene/low-molecular-weight polyethylene blend for artificial joint application.

    PubMed

    Xu, Ling; Chen, Chen; Zhong, Gan-Ji; Lei, Jun; Xu, Jia-Zhuang; Hsiao, Benjamin S; Li, Zhong-Ming

    2012-03-01

    An easy approach was reported to achieve high mechanical properties of ultrahigh-molecular-weight polyethylene (UHMWPE)-based polyethylene (PE) blend for artificial joint application without the sacrifice of the original excellent wear and fatigue behavior of UHMWPE. The PE blend with desirable fluidity was obtained by melt mixing UHMWPE and low molecular weight polyethylene (LMWPE), and then was processed by a modified injection molding technology-oscillatory shear injection molding (OSIM). Morphological observation of the OSIM PE blend showed LMWPE contained well-defined interlocking shish-kebab self-reinforced superstructure. Addition of a small amount of long chain polyethylene (2 wt %) to LMWPE greatly induced formation of rich shish-kebabs. The ultimate tensile strength considerably increased from 27.6 MPa for conventional compression molded UHMWPE up to 78.4 MPa for OSIM PE blend along the flow direction and up to 33.5 MPa in its transverse direction. The impact strength of OSIM PE blend was increased by 46% and 7% for OSIM PE blend in the direction parallel and vertical to the shear flow, respectively. Wear and fatigue resistance were comparable to conventional compression molded UHMWPE. The superb performance of the OSIM PE blend was originated from formation of rich interlocking shish-kebab superstructure while maintaining unique properties of UHMWPE. The present results suggested the OSIM PE blend has high potential for artificial joint application.

  4. 78 FR 9363 - Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic of China: Notice of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-02-08

    ...., Ltd. v. United States, Slip Op. 13-10 (CIT 2013).\\1\\ \\1\\ See Final Results of Redetermination Pursuant.../remands (``PET Film Final Remand''); see also Fuwei Films (Shandong) Co., Ltd. v. United States, Consol... decision of the United States Court of Appeals for the Federal Circuit (``CAFC'') in Timken Co. v....

  5. Physicochemical and mechanical properties of experimental coextruded food-packaging films containing a buried layer of recycled low-density polyethylene.

    PubMed

    Badeka, Anastasia; Goulas, Antonios E; Adamantiadi, Antigoni; Kontominas, Michael G

    2003-04-09

    Migrational, permeation, and tensile properties of experimental five- and eight-layer coextruded and laminated films containing a middle buried layer of recycled low-density polyethylene (LDPE) comprising 40-50% bw of the multilayer structure were determined. Respective films containing 100% virgin LDPE as the buried layer were taken as controls. Results showed that the percentage of recycled LDPE in the multilayer structure did not affect overall migration values to distilled water, 3% acetic acid, and iso-octane. In all cases, overall migration values were lower than the upper acceptable limit (10 mg/dm(2)) set by the European Union. Transmission rate values to O(2), CO(2), and water vapor were also not affected by the percentage of recycled LDPE in the multilayer structure. On the basis of O(2) transmission rates, low-barrier, barrier, and high-barrier multilayer structures were produced. Likewise, tensile properties (tensile strength, percent elongation at break, and Young's modulus) were not affected by the percentage of recycled material in the multilayer structure. Finally, all experimental films produced no adverse effects in taste or odor of the food-contacting phase tested. The above findings are discussed in relation to the high quality of the primary LDPE scrap used throughout this work in combination with the functional barrier hypothesis. On the basis of the present results it is proposed that primary LDPE scrap may be used as a middle layer comprising 40-50% bw of multilayer food-packaging films without any compromise in migrational, barrier, mechanical, and organoleptic properties.

  6. Preparation and characterization of gradient polymer films

    SciTech Connect

    Smith, S.C.

    1987-01-01

    Gradient polymers are multicomponent polymers whose chemical constitution varies with depth in the sample. Although these polymers may possess unique mechanical, optical, and barrier properties they remain relatively unexplored. This work is a study of the preparation of gradient polymers by sequential exposure of films to a diffusing monomer followed by electron beam irradiation. Initial experiments involved immersion of poly(vinyl chloride) (PVC) films in styrene or n-butyl methacrylate (BMA) for various time periods followed by irradiation with 1 or 10 megarads of accelerated electrons. A significant amount of poly(n-butyl methacrylate) (PBMA) formed in PVC/BMA systems, but little polystyrene could be found in the PVC/styrene films. A second set of experiments involved immersion of PVC and polyethylene (PE) films in BMA for 20, 40, 60, and 720 minutes followed by irradiation with 10 megarads of electrons. These films were then characterized using optical microscopy, quantitative transmission Fourier transform infrared spectroscopy (FTIR), and a depth profiling procedure based on quantitative attenuated total reflection (ATR) FTIR. It was concluded that the mechanism of PBMA formation in the polyethylene films was a result of events immediately following irradiation. Atmospheric oxygen diffusing into irradiated films trapped free radicals at the film surfaces. This was followed by storage in an evacuated desiccator where unintentional exposure to BMA vapor took place. This BMA reacted with free radicals that remained within the film cores, polymerizing to PBMA.

  7. Autoantibodies to phosphatidylethanolamine (PE) recognize a kininogen-PE complex.

    PubMed

    Sugi, T; McIntyre, J A

    1995-10-15

    Demonstration of autoimmune antiphospholipid antibodies (aPA) to negatively charged phospholipids (PL) in an enzyme-linked immunosorbent assay (ELISA) requires the presence of certain phospholipid-binding plasma proteins, eg, beta 2-glycoprotein I. We found a requirement for plasma against the electrically neutral or zwitterionic phospholipid, phosphatidylethanolamine (PE). Two of these PE-binding plasma proteins were identified as high molecular weight kininogen (HMWK) and low molecular weight kininogen (LMWK). We studied anti-PE antibody (aPE) seropositive plasma from 13 patients with SLE and/or recurrent spontaneous abortions by using partially purified kininogens and kininogen binding proteins from adult bovine serum isolated by carboxymethyl (CM)-papain affinity chromatography. Eleven of 13 sera recognized a kininogen-PE complex and/or a kininogen-binding protein-kininogen-PE complex. Some aPE-positive patient sera were shown to recognize highly purified HMWK and LMWK by ELISA only when the kininogens were presented on a PE substrate. These aPE sera did not recognize PE, HMWK, or LMWK when they were presented independently as the sole antigens on the ELISA plates. Other aPE-positive sera that did not react with PE-bound HMWK or LMWK reacted with the CM-papain column eluate when it was bound to PE, which suggests that these aPE recognize factor XI or prekallikrein, which normally bind to HMWK. The aPE ELISA reactivity of two patient sera were inhibited by preincubation of the CM-papain column eluate in the ELISA plate. These data show that most aPE are not specific for PE but require the presence of certain PL-binding plasma proteins that are kininogens or proteins in complex with kininogens. Our studies indicate that aPE bind to different plasma proteins than those implicated in anionic PL, aPA ELISA reactivity.

  8. Statistical analysis of the strength of ultra-oriented ultra-high-molecular-weight polyethylene film filaments in the framework of the Weibull model

    NASA Astrophysics Data System (ADS)

    Boiko, Yu. M.; Marikhin, V. A.; Myasnikova, L. P.; Moskalyuk, O. A.; Radovanova, E. I.

    2016-10-01

    A statistical analysis of the distribution of the tensile strength σ of ultra-oriented ultra-high-molecular-weight polyethylene (UHMWPE) film filaments has been performed in the framework of the Weibull model using the results obtained from a large number (50) of measurements. The UHMWPE film filaments have been produced by means of high-temperature multistage zone drawing of xerogels prepared from 1.5% UHMWPE solutions in decalin. The Weibull modulus has been determined for this type of materials. It has been shown that, for the ultimate draw ratio λ = 120, the average tensile strength is equal to 4.7 GPa, which is significantly higher than the tensile strength σ = 3.5 GPa for commercial gel-spun UHMWPE fibers manufactured by the DSM Company (The Netherlands) and the Honeywell International Incorporation (United States). It has been demonstrated that, for 20% of the specimens thus prepared, the tensile strength reaches record-high values σ = 5.2-5.9 GPa.

  9. β - NMR Measurements of Lithium Ion Transport in Thin Films of Pure and Lithium-Salt-Doped Poly(ethylene oxide)

    NASA Astrophysics Data System (ADS)

    McKenzie, Iain; Harada, Masashi; Cortie, David L.; Kiefl, Robert F.; Levy, C. D. Philip; Macfarlane, W. Andrew; McFadden, Ryan M. L.; Morris, Gerald D.; Ogata, Shin-Ichi; Pearson, Matthew R.; Sugiyama, Jun

    2015-03-01

    β - Detected nuclear spin relaxation of 8Li+ has been used to study the microscopic diffusion of lithium ions in thin films of poly(ethylene oxide) (PEO), PEO with lithium bis(trifluoromethanesulfonyl)imide (LiTFSI), PEO with lithium triflate (LiTf) and PEO with lithium trifluoroacetic acid (LiTFA) with monomer-to-salt ratios of 8.3:1. Hopping of Li + above ~ 250 K follows an Arrhenius law in all of the films. Diffusion of Li+ is fastest in pure PEO and decreases in order LiTFSI >LiTf >LiTFA. We observed the activation energy for hopping (EA) and the intrinsic hop rate (τ0-1) both increasing in order LiTFA

  10. Temperature, pressure critical in PE line pipe use

    SciTech Connect

    Oney, C.L.

    1988-01-01

    Polyethylene (PE) line pipe is used for low-pressure gas (gathering, supply gas, etc.) and water lines and, in some cases for flow lines. API Spec 15LE specifies minimum requirements for qualification of product and quality control by manufacturers of polyethylene pipe. Spec 15LE also provides guidelines for design of polyethylene. Thermoplastic pipe (PE and PVC) is manufactured by melting resin pellets or powder and extruding the melt through dies. Thermoplastic pipe pressure classes are designated by ''standard dimension ratios'' (SDR). The SDR is the average OD divided by the wall thickness (w.t.). Thus 2 3/8-in. OD pipe (nominal 2 in.) with 0.216-in. w.t. is SDR 11. Nominal 3-in. pipe (3 1/2-in. OD) must have a minimum 0.318-in. w.t. to be SDR 11. Table 5.1 in Spec 15LE lists the most commonly used SDRs. Quality control during manufacture required by Spec 15LE for PE pipe includes short-term hydrostatic tests and dimensional checks. Frequency of tests depend on whether the pipe is coiled or cut into lengths. PE pipe sizes of 3 in. and smaller sizes usually are coiled. In addition, annual tests for verification of long-term pressure rating are required by Spec 15LE.

  11. The interplay of plasma treatment and gold coating and ultra-high molecular weight polyethylene: On the cytocompatibility.

    PubMed

    Novotná, Zdenka; Rimpelová, Silvie; Juřík, Petr; Veselý, Martin; Kolská, Zdenka; Hubáček, Tomáš; Ruml, Tomáš; Švorčík, Václav

    2017-02-01

    We have investigated the application of Ar plasma for creation of nanostructured ultra high molecular weight polyethylene (PE) surface in order to enhance adhesion of mouse embryonic fibroblasts (L929). The aim of this study was to investigate the effect of the interface between plasma-treated and gold-coated PE on adhesion and spreading of cells. The surface properties of pristine samples and its modified counterparts were studied by different experimental techniques (gravimetry, goniometry and X-ray photoelectron spectroscopy (XPS), electrokinetic analysis), which were used for characterization of treated and sputtered layers, polarity and surface chemical structure, respectively. Further, atomic force microscopy (AFM) was employed to study the surface morphology and roughness. Biological responses of cells seeded on PE samples were evaluated in terms of cell adhesion, spreading, morphology and proliferation. Detailed cell morphology and intercellular connections were followed by scanning electron microscopy (SEM). As it was expected the thickness of a deposited gold film was an increasing function of the sputtering time. Despite the fact that plasma treatment proceeded in inert plasma, oxidized degradation products were formed on the PE surface which would contribute to increased hydrophilicity (wettability) of the plasma treated polymer. The XPS method showed a decrease in carbon concentration with increasing plasma treatment. Cell adhesion measured on the interface between plasma treated and gold coated PE was inversely proportional to the thickness of a gold layer on a sample.

  12. Deposition of plasma polymerized perfluoromethylene-dominated films showing oil-repellency

    NASA Astrophysics Data System (ADS)

    Chase, J. E.; Boerio, F. J.

    2003-05-01

    Plasma polymerized fluorocarbon films were deposited onto polyethylene (PE) substrates to increase oil-repellency of PE. Depositions were performed using the monomer, 1H,1H,2H-perfluoro-1-dodecene in a parallel-plate, radio frequency (rf) reactor, with variable continuous-wave power ranging from 2 to 160 W. The film deposition rate and morphology were strongly dependent on the applied rf power. Most importantly, the chemical structure of the deposited films was also altered, resulting in changes in contact angles of various liquids and the surface energy. Films deposited at low power were composed mainly of perfluoromethylene (CF2) species (up to 67.2%), as shown by x-ray photoelectron spectroscopy (XPS). With an increase in rf power, CF2 content in the film decreased as further fragmentation of the monomer occurred. For each deposition at varying rf powers, even at powers as low as 2 W, the C=C and C-H bonds in the monomer were dissociated by the plasma and not incorporated into the films, as shown by Fourier transform infrared spectroscopy. Oil-repellency, as shown by increased contact angles of hydrocarbon liquids, was found to increase as the amount of CF2 species increased in the film structure. A low critical surface energy (2.7 mJ/m2) was calculated for the film deposited with only 2 W of rf power. Adhesion of the plasma-polymerized films to the PE was also evaluated and found to be poor for films with a high concentration of CF2 species, where cohesive failure within the film occurred. However, adhesion increased as a function of rf power, where the film structure showed more cross-linking. There was a compromise between producing a film with high oleophobicity (oil-repellency) while maintaining adhesion of the film to PE, as some disruption of the CF2 chains in the films was necessary for cohesion through cross-linking.

  13. Design procedure prevents PE pipe rupture

    SciTech Connect

    Grigory, S.C.

    1995-12-01

    A rupture prevention design procedure for plastic gas distribution pipe is nearing completion at Southwest Research Institute (SWRI). Given the pipe size, polyethylene (PE) resin, and minimum operating temperature, the maximum safe operating pressure can be determined for which rapid crack propagation (RCP) cannot occur. A computer program, called PFRAC, has been developed for this purpose and uses Charpy energy as the measurement of fracture toughness of PE. Present efforts, however, involve replacing Charpy energy with a dynamic toughness measurement obtained from the Small Scale Steady State (S4) test that is required in ISO 4437. The program is being financed by the Gas Research Institute, Chicago. RCP events in PE pipe have been rare primarily because operating pressures are low and pipe diameters are small in most gas distribution systems. However, controlled RCP experiments in the US and other countries clearly demonstrate that as the gas industry moves toward higher line pressures and larger diameters, the likelihood of an RCP event increases. Recognizing this, ISO includes a requirement for RCP in its ISO 4437 standard for pipe greater than 10 inches in diameter or operating pressures greater than 58 psig. The S4 test may be used on all pipe diameters. A full scale test or the S4 test can be used on pipe greater than 10 inches diameter.

  14. In Situ Nanocalorimetric Investigations of Plasma Assisted Deposited Poly(ethylene oxide)-like Films by Specific Heat Spectroscopy.

    PubMed

    Madkou, Sherif; Melnichu, Iurii; Choukourov, Andrei; Krakovsky, Ivan; Biederman, Hynek; Schönhals, Andreas

    2016-04-28

    In recent years, highly cross-linked plasma polymers have started to unveil their potential in numerous biomedical applications in thin-film form. However, conventional diagnostic methods often fail due to their diverse molecular dynamics conformations. Here, glassy dynamics and the melting transition of thin PEO-like plasma assisted deposited (ppPEO) films (thickness 100 nm) were in situ studied by a combination of specific heat spectroscopy, utilizing a pJ/K sensitive ac-calorimeter chip, and composition analytical techniques. Different cross-linking densities were obtained by different plasma powers during the deposition of the films. Glassy dynamics were observed for all values of the plasma power. It was found that the glassy dynamics slows down with increasing the plasma power. Moreover, the underlying relaxation time spectra broaden indicating that the molecular motions become more heterogeneous with increasing plasma power. In a second set of the experiment, the melting behavior of the ppPEO films was studied. The melting temperature of ppPEO was found to decrease with increasing plasma power. This was explained by a decrease of the order in the crystals due to formation of chemical defects during the plasma process.

  15. Low-temperature layer transfer of midair cavity silicon films to a poly(ethylene terephthalate) substrate by meniscus force

    NASA Astrophysics Data System (ADS)

    Sakaike, Kohei; Nakamura, Shogo; Akazawa, Muneki; Higashi, Seiichiro

    2014-01-01

    A single-crystalline-silicon (c-Si) layer (supported by columns on a starting Si-on-insulator wafer) and a counter-poly(ethylene terephthalate) (PET) substrate were placed in close face-to-face contact, and pure water was sandwiched in between the c-Si layer and the PET substrate. The samples formed in this manner were heated on a hot plate at 80 °C. By the meniscus force generated during the evaporation of the sandwiched water from the samples, the c-Si films were completely transferred to the PET substrate. A (100)-oriented c-Si thin film that shows good adhesion was successfully formed on PET substrates at low process temperatures.

  16. Q-switched erbium doped fiber laser based on single and multiple walled carbon nanotubes embedded in polyethylene oxide film as saturable absorber

    NASA Astrophysics Data System (ADS)

    Ahmed, M. H. M.; Ali, N. M.; Salleh, Z. S.; Rahman, A. A.; Harun, S. W.; Manaf, M.; Arof, H.

    2015-01-01

    A passive, stable and low cost Q-switched Erbium-doped fiber laser (EDFL) is demonstrated using both single-walled carbon nanotubes (SWCNTs) and multi-walled carbon nanotubes (MWCNTs), which are embedded in polyethylene oxide (PEO) film as a saturable absorber (SA). The film is sandwiched between two FC/PC fiber connectors and integrated into the laser cavity for Q-switching pulse generation operating at wavelength of 1533.6 nm. With SWCNTs, the laser produces a stable pulse train with repetition rate and pulse width ranging from 9.52 to 33.33 kHz and 16.8 to 8.0 μs while varying the 980 nm pump power from 48.5 mW to 100.4 mW. On the other hand, with MWCNTs, the repetition rate and pulse width can be tuned in a wider range of 6.12-33.62 kHz and 9.5- 4.2 μs, respectively as the pump power increases from 37.9 to 120.6 mW. The MWCNTs produce the pulse train at a lower threshold and attain a higher repetition rate compared to the SWCNTs. This is due to thicker carbon nanotubes layer of the MWCNTs which provides more absorption and consequently higher damage threshold. The Q-switched EDFL produces the highest pulse energy of 531 nJ at pump power of 37.9 mW with the use of MWCNTs-PEO SA.

  17. β-NMR measurements of lithium ion transport in thin films of pure and lithium-salt-doped poly(ethylene oxide).

    PubMed

    McKenzie, Iain; Harada, Masashi; Kiefl, Robert F; Levy, C D Philip; MacFarlane, W Andrew; Morris, Gerald D; Ogata, Shin-Ichi; Pearson, Matthew R; Sugiyama, Jun

    2014-06-04

    β-Detected nuclear spin relaxation of (8)Li(+) has been used to study the microscopic diffusion of lithium ions in thin films of poly(ethylene oxide) (PEO), where the implanted lithium ions are present in extremely low concentration, and PEO with 30 wt % LiCF3SO3 over a wide range of temperatures both above and below the glass transition temperature. Recent measurements by Do et al. [Phys. Rev. Lett. 2013, 111, 018301] found that the temperature dependence of the Li(+) conductivity was identical to that of the dielectric α relaxation and was well described by the Vogel-Fulcher-Tammann relation, implying the α relaxation dominates the Li(+) transport process. In contrast, we find the hopping of Li(+) in both samples in the high temperature viscoelastic phase follows an Arrhenius law and depends significantly on the salt content. We propose that the hopping of Li(+) between cages involves motion of the polymer but that it is only for long-range diffusion where the α relaxation plays an important role.

  18. Formulation and in vitro characterization of novel sildenafil citrate-loaded polyvinyl alcohol-polyethylene glycol graft copolymer-based orally dissolving films.

    PubMed

    Xu, Li-Li; Shi, Li-Li; Cao, Qing-Ri; Xu, Wei-Juan; Cao, Yue; Zhu, Xiao-Yin; Cui, Jing-Hao

    2014-10-01

    This work was aimed to develop novel sildenafil citrate (SC)-loaded polyvinyl alcohol (PVA)-polyethylene glycol (PEG) graft copolymer (Kollicoat(®) IR)-based orally dissolving films (ODFs) using a solvent casting method. Formulation factors such as plasticizers and disintegrants were optimized on the basis of characteristics of blank ODFs. The SC-loaded ODF with a loading capacity up to 6.25mg in an area of 6 cm(2) was prepared and evaluated in terms of mechanical properties, disintegration time and dissolution rate. The physicochemical properties of drug-loaded ODF were also investigated using the scanning electron microscope (SEM), X-ray diffraction (XRD), differential scanning calorimetry (DSC) and Fourier transform infrared spectroscopy (FT-IR). The blank ODF composed of Kollicoat(®) IR, sodium alginate (ALG-Na) and glycerol (10:2:1.5, w/w) had a remarkably short disintegration time of about 20s. The SC-loaded ODF showed a delayed disintegration time (about 25s), but exhibited improved mechanical properties when compared to the blank ODF. SC was homogeneously dispersed throughout the ODF and the crystalline form of drug had been partly changed, existing strong hydrogen bonding between the drug and carriers. The Kollicoat(®) IR/ALG-Na based ODFs containing SC might be an alternative to conventional tablet for the treatment of male erectile dysfunction.

  19. Ca2+ and Mg2+ binding site engineering increases the degradation of polyethylene terephthalate films by polyester hydrolases from Thermobifida fusca.

    PubMed

    Then, Johannes; Wei, Ren; Oeser, Thorsten; Barth, Markus; Belisário-Ferrari, Matheus R; Schmidt, Juliane; Zimmermann, Wolfgang

    2015-04-01

    Several bacterial polyester hydrolases are able to hydrolyze the synthetic polyester polyethylene terephthalate (PET). For an efficient enzymatic degradation of PET, reaction temperatures close to the glass transition temperature of the polymer need to be applied. The esterases TfH, BTA2, Tfu_0882, TfCut1, and TfCut2 produced by the thermophilic actinomycete Thermobifida fusca exhibit PET-hydrolyzing activity. However, these enzymes are not sufficiently stable in this temperature range for an efficient degradation of post-consumer PET materials. The addition of Ca2+ or Mg2+ cations to the enzymes resulted in an increase of their melting points between 10.8 and 14.1°C determined by circular dichroism spectroscopy. The thermostability of the polyester hydrolases was sufficient to degrade semi-crystalline PET films at 65°C in the presence of 10 mM Ca2+ and 10 mM Mg2+ resulting in weight losses of up to 12.9% after a reaction time of 48 h. The residues Asp174, Asp204, and Glu253 were identified by molecular dynamics simulations as potential binding residues for the two cations in TfCut2. This was confirmed by their substitution with arginine, resulting in a higher thermal stability of the corresponding enzyme variants. The generated variants of TfCut2 represent stabilized catalysts suitable for PET hydrolysis reactions performed in the absence of Ca2+ or Mg2+.

  20. Simulation of synaptic short-term plasticity using Ba(CF3SO3)2-doped polyethylene oxide electrolyte film

    PubMed Central

    Chang, C. T.; Zeng, F.; Li, X. J.; Dong, W. S.; Lu, S. H.; Gao, S.; Pan, F.

    2016-01-01

    The simulation of synaptic plasticity using new materials is critical in the study of brain-inspired computing. Devices composed of Ba(CF3SO3)2-doped polyethylene oxide (PEO) electrolyte film were fabricated and with pulse responses found to resemble the synaptic short-term plasticity (STP) of both short-term depression (STD) and short-term facilitation (STF) synapses. The values of the charge and discharge peaks of the pulse responses did not vary with input number when the pulse frequency was sufficiently low(~1 Hz). However, when the frequency was increased, the charge and discharge peaks decreased and increased, respectively, in gradual trends and approached stable values with respect to the input number. These stable values varied with the input frequency, which resulted in the depressed and potentiated weight modifications of the charge and discharge peaks, respectively. These electrical properties simulated the high and low band-pass filtering effects of STD and STF, respectively. The simulations were consistent with biological results and the corresponding biological parameters were successfully extracted. The study verified the feasibility of using organic electrolytes to mimic STP. PMID:26739613

  1. Quantitative investigation of the photodegradation of polyethylene terephthalate film by friction force microscopy, contact-angle goniometry, and X-ray photoelectron spectroscopy.

    PubMed

    Hurley, Claire R; Leggett, Graham J

    2009-08-01

    Studies of the UV-induced photodegradation of poly(ethylene terephthalate) (PET) have been carried out using contact-angle goniometry, X-ray photoelectron spectroscopy (XPS), and friction force microscopy (FFM). The advancing contact angle of water, theta, decreased following exposure of free-standing PET films to UV light. Measurements of surface friction by FFM showed that the coefficient of friction mu increased as the degradation proceeded, reaching a limiting value after ca 200 min, in agreement with the contact angle data. Using a modified form of the Cassie equation, a quantitative analysis of the extent of modification could be carried out. There was a very close correlation between the coefficient of friction determined by FFM and the value of cos theta. XPS provided more detailed information on surface bonding that also correlated closely with the FFM data. Although FFM provides quantitative data on surface modification with nanometer-scale spatial resolution, it does not provide detailed structural information such as is provided by XPS. The oxygen content at the surface was found to increase as photo-generated radicals within the PET reacted with atmospheric oxygen. Increases in both ester and carbonyl contributions within XPS data accompanied this increase. It was concluded that the photodegradation process follows mainly Norrish type I reaction pathways, following previous work by Fechine et al and Grosstete et al.

  2. Shock induced dissociation of polyethylene

    SciTech Connect

    Morris, C.E.; Loughran, E.D.; Mortensen, G.F.; Gray, G.T. III; Shaw, M.S.

    1989-01-01

    To identify the physical processes occurring on the Hugoniot, shock-recovery experiments were performed. Cylindrical recovery systems were used that enabled a wide range of single-shock Hugoniot states to be examined. Mass spectroscopy was used to examine the gaseous dissociation products. X-ray and TEM measurements were made to characterize the post-shock carbon structures. A dissociation product equation of state is presented to interpret the observed results. Polyethylene (PE) samples that were multiply shocked to their final states dissociated at much higher pressures than single-shocked samples. 5 refs., 2 figs., 1 tab.

  3. TG/FTIR analysis on co-pyrolysis behavior of PE, PVC and PS.

    PubMed

    Wu, Jingli; Chen, Tianju; Luo, Xitao; Han, Dezhi; Wang, Zhiqi; Wu, Jinhu

    2014-03-01

    The pyrolysis and co-pyrolysis behaviors of polyethylene (PE), polystyrene (PS) and polyvinyl chloride (PVC) under N2 atmosphere were analyzed by Thermal gravimetric/Fourier transform infrared (TG/FTIR). The volatile products were analyzed to investigate the interaction of the plastic blends during the thermal decomposition process. The TGA results showed that the thermal stability increased followed by PVC, PS and PE. The pyrolysis process of PE was enhanced when mixed with PS. However, PS was postponed when mixed with PVC. As for PE and PVC, mutual block was happened when mixed together. The FTIR results showed that the free radical of the decomposition could combine into a stable compound. When PE mixed with PVC or PS, large amount of unsaturated hydrocarbon groups existed in products while the content of alkynes was decreased. The methyl (-CH3) and methylene (-CH2-) bonds were disappeared while PVC mixed with PE.

  4. Yield Stress Enhancement in Glassy-Polyethylene Block Copolymers

    NASA Astrophysics Data System (ADS)

    Mulhearn, William; Register, Richard

    Polyethylene (PE) has the highest annual production volume of all synthetic polymers worldwide, and is valuable across many applications due to its low cost, toughness, processability, and chemical resistance. However, PE is not well suited to certain applications due to its modest yield stress and Young's modulus (approximately 30 MPa and 1 GPa, respectively for linear, high-density PE). Irreversible deformation of PE results from dislocation of crystal stems and eventual crystal fragmentation under applied stress. The liquid-like amorphous fraction provides no useful mechanical support to the crystal fold surface in a PE homopolymer, so the only method to enhance the force required for crystal slip, and hence the yield stress, is crystal thickening via thermal treatment. An alternative route towards modifying the mechanical properties of PE involves copolymerization of a minority high-glass transition temperature block into a majority-PE block copolymer. In this work, we investigate a system of glassy/linear-PE block copolymers prepared via ring-opening metathesis polymerization of cyclopentene and substituted norbornene monomers followed by hydrogenation. We demonstrate that a large change in mechanical properties can be achieved with the addition of a short glassy block (e.g. a doubling of the yield stress and Young's modulus versus PE homopolymer with the addition of 25 percent glassy block). Furthermore, owing to the low interaction energy between PE and the substituted polynorbornene blocks employed, these high-yield PE block copolymers can exhibit single-phase melts for ease of processability.

  5. Radiation resistivity of polyacenaphthylene-grafted polyethylene

    NASA Astrophysics Data System (ADS)

    Hayakawa, Kiyoshi; Kawase, Kaoru; Yamakita, Hiromi

    Thin poly (ethylene-g-acenaphthylene) films prepared by the vapor-phase grafting method were subjected to the γ-irradiation in air, and various changes in tensile and structural properties of the film were investigated by comparing with those of the untreated or crosslinked polyethylene film. Polyethylene got to lose its inherent necking property by oxidative degradation and to be brittle-fractured by the irradiation dose less than 100 Mrad in air. The polyacenaphthylene-grafted polyethylenes (extent of grafting, ˜ 54 by {100( P-P°) }/{P°}), however, kept their ductility up to 200 Mrad or more, and the rate of increase in elastic modulus as well as yield strength with the increasing irradiation dose was considerably lower than that of untreated or crosslinked polyethylene. The effect of the grafting extent, and that of the irradiation dose-rate on the fracture energy were also examined. The weight increase of polyethylene due to the oxygen consumption and the resulting formation of carbonyl group which proceeded proportionally with the irradiation dose were remarkably suppressed by the grafting, whereas the double bond formation seemed to be unaffected by it. The grafted film held the original content of gel fraction unchanged during the irradiation in air, but the average molecular weight of the sol fraction decreased gradually. Meanwhile, the gel fraction of the crosslinked polyethylene was degenerated by a small dose of irradiation. The analysis of gaseous products revealed the formation of water, methanol, acetaldehyde and so forth from the irradiated grafted film. The grafting procedure and the subsequent irradiation of the grafted film did not affect the degree of crystallinity of the backbone polyethylene. The role played by the grafted polyacenaphthylene for endowing the radiation resistivity to polyethylene and its inherent limitation in effect were discussed from the structural point of view of the grafted film.

  6. Effect of amine functionalized polyethylene on clay-silver dispersion for polyethylene nanocomposites

    NASA Astrophysics Data System (ADS)

    Sánchez-Valdes, S.; Ibarra-A, M. C.; Ramírez-V, E.; Ramos-V, L. F.; Martinez-C, J. G.; Romero-G, J.; Ledezma-P, A. S.; Rodriguez-F, O. S.

    2014-08-01

    The compatibilization provided by maleic anhydride (MA) and 2-[2-(dimethylamino)-ethoxy] ethanol (DMAE) functionalized polyethylene for forming polyethylene-based nanocomposites was studied and compared. MA was grafted into PE by melt mixing to obtain PEgMA (compatibilizer 1), thereafter, PEgMA was reacted with DMAE and an antioxidant also by melt mixing to obtain PAgDMAE (compatibilizer 2). These compatibilizers were reacted using ultrasound with a solution of AgNO3 0.04 M and Ethylene glycol. Ammonium hydroxide was added in a ratio of 2:1 molar with respect to silver nitrate. These silver coated compatibilizers were mixed with PE and nano-clay (Cloisite I28E), thus forming the different hybrid PE-clay-silver nanocomposites. FTIR confirmed the formation of these two compatibilizers. All the compatibilized nanocomposites had better filler (clay and silver) dispersion and exfoliation compared to the uncompatibilized PE nanocomposites. X-ray diffraction, mechanical and antimicrobial properties attained showed that the PEgDMAE produced the better dispersed PE, clay and silver nanocomposites. The obtained nanocomposites showed outstanding antimicrobial properties against bacteria, Escherichia coli and fungus, Aspergillus niger. It is concluded that the PEgDMAE offers an outstanding capability for preparing nanocomposites with highly exfoliated and dispersed filler into the PE matrix.

  7. Development of indigenous linear low-density polyethylene film and other related techniques for heavy-load balloons in India

    NASA Astrophysics Data System (ADS)

    Redkar, R. T.

    1993-02-01

    A new grade of balloon film extruded out of LLDPE resin with Butene as comonomer and Cold Brittle Point (CBP) at -88°C was extruded and successfully flight tested with a 25 micron single shell 53,000 Cu.M. balloon carrying 330 Kg. payload to 33 Km. altitude. We have also produced superior LLDPE film out of Dowlex 2045 Dow Chemicals resin with Octene as comonomer, which has the cold brittle point lower than -90°C and superior mechanical properties at low temperatures. A high pressure hydrogen filling system capable of delivering 2200 Cu.Ft. of hydrogen per minute has been commissioned and successfully utilised in 11 flights. With this new filling system, the inflation time is drastically reduced by over 50% thereby reducing the duration of pre-launch stresses on the ground bubble. After the acceptance of our revised design criteria for balloons to be flown from equatorial latitudes by M/s.Winzen International Inc., U.S.A., 41 flights have been made, out of which 36 have been successful giving us a success record of 88%. Out of the 5 failures, 3 have been float failures with gross inflations exceeding 1950 kg, for which launch spool damage is a suspect. To reduce the spool damage, the shell thickness of the subsequent balloon was increased to 20.32 microns from 17.78 microns and the flight was a success. For further reducing the possibility of launch spool damage, a larger diameter spool is being designed.

  8. Conversion of post-industrial PET-PE scraps into compatibilized plastic blends for new applications

    NASA Astrophysics Data System (ADS)

    Bartoli, Flavia; Bruni, Cosimo; Coltelli, Maria-Beatrice; Castelvetro, Valter; Ciardelli, Francesco

    2012-07-01

    Poly(ethylene terephthalate) (PET) / poly(ethylene) (PE) granules coming from a post-industrial packaging stream were directed to new applications. The collected material was first characterized through selective extractions followed by infrared analysis. After the characterization work the presence of poly(ethylene-co-vinyl acetate) (EVA) copolymer was evidenced. Moreover the degree of yellowing was shown to increase by increasing the PE content in the granules batch. The blending of PET/PE with a stabilizer allowed to control its thermal stability, moreover the addition of compatibilizers resulted in the possibility of modulating both rheological and mechanical properties. Hence the use of stabilizers and compatibilizers allowed to upgrade postindustrial PET/PE based materials for the use in different industrial applications

  9. Profiles in garbage: Polyethylene terephthalate

    SciTech Connect

    Miller, C.

    1997-11-01

    Polyethylene terephthalate (PET) is a plastic resin used primarily to make bottles. Soft drinks -- along with salad dressing, fruit juices, peanut butter, and other household and consumer products -- use PET bottles. PET also is used for film, sheeting for cups and food trays, oven-safe trays, and other uses. PET is a relatively new packaging resin, first commercialized in the early 1970s. Because it is an ``engineered`` resin, PET is more expensive than commodity resins such as high-density polyethylene (HDPE) and, for the same reason, it is usually the highest valued plastic recyclable.

  10. Development of TLSER model and QSAR model for predicting partition coefficients of hydrophobic organic chemicals between low density polyethylene film and water.

    PubMed

    Liu, Huihui; Wei, Mengbi; Yang, Xianhai; Yin, Cen; He, Xiao

    2017-01-01

    Partition coefficients are vital parameters for measuring accurately the chemicals concentrations by passive sampling devices. Given the wide use of low density polyethylene (LDPE) film in passive sampling, we developed a theoretical linear solvation energy relationship (TLSER) model and a quantitative structure-activity relationship (QSAR) model for the prediction of the partition coefficient of chemicals between LDPE and water (Kpew). For chemicals with the octanol-water partition coefficient (log Kow) <8, a TLSER model with Vx (McGowan volume) and qA(-) (the most negative charge on O, N, S, X atoms) as descriptors was developed, but the model had relatively low determination coefficient (R(2)) and cross-validated coefficient (Q(2)). In order to further explore the theoretical mechanisms involved in the partition process, a QSAR model with four descriptors (MLOGP (Moriguchi octanol-water partition coeff.), P_VSA_s_3 (P_VSA-like on I-state, bin 3), Hy (hydrophilic factor) and NssO (number of atoms of type ssO)) was established, and statistical analysis indicated that the model had satisfactory goodness-of-fit, robustness and predictive ability. For chemicals with log KOW>8, a TLSER model with Vx and a QSAR model with MLOGP as descriptor were developed. This is the first paper to explore the models for highly hydrophobic chemicals. The applicability domain of the models, characterized by the Euclidean distance-based method and Williams plot, covered a large number of structurally diverse chemicals, which included nearly all the common hydrophobic organic compounds. Additionally, through mechanism interpretation, we explored the structural features those governing the partition behavior of chemicals between LDPE and water.

  11. Low-density polyethylene films treated by an atmospheric Ar-O2 post-discharge: functionalization, etching, degradation and partial recovery of the native wettability state

    NASA Astrophysics Data System (ADS)

    Abou Rich, S.; Dufour, T.; Leroy, P.; Nittler, L.; Pireaux, J. J.; Reniers, F.

    2014-02-01

    To optimize the adhesion of layers presenting strong barrier properties on low-density polyethylene (LDPE) surfaces, we investigated the influence of argon and argon-oxygen atmospheric pressure post-discharges. This study was performed using x-ray photoelectron spectroscopy, atomic force microscopy, optical emission spectroscopy (OES) and dynamic water contact angle (WCA) measurements. After the plasma treatment, a slight increase in the roughness was emphasized, more particularly for the samples treated in a post-discharge supplied in oxygen. Measurements of the surface roughness and of the oxygen surface concentration suggested the competition of two processes playing a role on the surface hydrophilicity and occurring during the post-discharge treatment: the etching and the activation of the surface. The etching rate was estimated to about 2.7 nm s-1 and 5.8 nm s-1 for Ar and Ar-O2 post-discharges, respectively. The mechanisms underlying this etching were investigated through experiments, in which we discuss the influence of the O2 flow rate and the distance (gap) separating the plasma torch from the LDPE surface located downstream. O atoms and NO molecules (emitting in the UV range) detected by OES seem to be good candidates to explain the etching process. An ageing study is also presented to evidence the stability of the treated surfaces over 60 days. After 60 days of storage, we showed that whatever the O2 flow rate, the treated films registered a loss of their hydrophilic state since their WCA increased towards a common threshold of 80°. This ‘hydrophobic recovery’ effect was mostly attributed to the reorientation of induced polar chemical groups into the bulk of the material. Indeed, the relative concentrations of the carbonyl and carboxyl groups at the surface decreased with the storage time and seemed to reach a plateau after 30 days.

  12. Radiation grafting of various water-soluble monomers on ultra-high molecular weight polyethylene powder. Part III: Preparation of compression moulded films, and water-uptake and morphological studies

    NASA Astrophysics Data System (ADS)

    Aydınlı, Bahattin; Tinçer, Teoman

    2001-10-01

    Compression moulded films were obtained from PAA, PMAA, PAAm, PNDAAm and PVP radiation grafted ultrahigh molecular weight polyethylene (UHMWPE) powders. Mechanical properties and water-uptake of PVP and PNDAAm grafted UHMWPE were found to be distinctly better than PAA, PMAA and PAAm ones. The former group showed almost complete melting and flow during compression moulding compared with the latter group. Hence, the mechanical properties of this group were found to be better than the others. Important parameters affecting the film formation appeared as H-bonding ability and also the compatibility between grafting polymer and UHMWPE. Per cent water-uptake of films increase with the grafting level and approaches 30% at most for all types of films except PMAA one. High per cent water-uptake results of PAA and PAAm cases should be taken cautiously due to incomplete flowing during compression in film preparation. SEM analysis revealed incomplete melting and flow for the case of PAA, PMAA and PAAm-co-UHMWPE resulting in pores and holes in the final films while homogeneous films were obtained for the case of PVP and PNDAAm.

  13. Polyethylene Glycol 3350

    MedlinePlus

    Polyethylene glycol 3350 is used to treat occasional constipation. Polyethylene glycol 3350 is in a class of medications ... Polyethylene glycol 3350 comes as a powder to be mixed with a liquid and taken by mouth. ...

  14. Polyethylene/organically-modified layered-silicate nanocomposites with antimicrobial activity

    NASA Astrophysics Data System (ADS)

    Songtipya, P.; Jimenez-Gasco, M. M.; Manias, E.

    2009-03-01

    Despite the very intensive research on polymer nanocomposites, the opportunities for new functionalities possible by nanofillers still remain largely untapped. Here, we present polyethylene/inorganic nanocomposites that exhibit strongly enhanced mechanical performance and, at the same time, also an antimicrobial activity originating from the organo-filler nature. Specifically, PE/organically-modified layered-silicate nanocomposites were prepared via melt-processing, and antimicrobial activity was designed by proper choice of their organic modification. Their antimicrobial activity was measured against three micotoxinogen fungal strains (Penicillium roqueforti and claviforme, and Fusarium graminearum) as model soil-borne plant and food contaminants. Montmorillonite-based organofillers, which only differ in their organic modification, were used to exemplify how these surfactants can be designed to render antifungal activity to the nanocomposites. The comparative discussion of the growth of fungi on unfilled PE and nanocomposite PE films is used to demonstrate how the antimicrobial efficacy is dictated by the surfactant chemistry and, further, how the nanocomposites' inhibitory activity compares to that of the organo-fillers and the surfactants.

  15. 76 FR 50456 - Notice of Final Results of Antidumping Duty Changed Circumstances Review: Polyethylene...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-08-15

    ...: Polyethylene Terephthalate Film, Sheet, and Strip From the Republic of Korea AGENCY: Import Administration... polyethylene terephthalate film, sheet, and strip (PET film) from Korea, effective as of the date of... Department published an antidumping duty order on PET film from Korea on June 5, 1991. See Antidumping...

  16. Determination of volatile organic compounds (VOCs) from wrapping films and wrapped PDO Italian cheeses by using HS-SPME and GC/MS.

    PubMed

    Panseri, Sara; Chiesa, Luca Maria; Zecconi, Alfonso; Soncini, Gabriella; De Noni, Ivano

    2014-06-25

    Nowadays food wrapping assures attractive presentation and simplifies self-service shopping. Polyvinylchloride (PVC)- and polyethylene (PE)-based cling-films are widely used worldwide for wrapping cheeses. For this purpose, films used in retail possess suitable technical properties such as clinginess and unrolling capacity, that are achieved by using specific plasticizers during their manufacturing process. In the present study, the main VOCs of three cling-films (either PVC-based or PE-based) for retail use were characterized by means of Solid-Phase Micro-Extraction and GC/MS. In addition, the effects of cling film type and contact time on the migration of VOCs from the films to four different PDO Italian cheeses during cold storage under light or dark were also investigated. Among the VOCs isolated from cling-films, PVC released 2-ethylhexanol and triacetin. These compounds can likely be considered as a "non-intentionally added substance". These same compounds were also detected in cheeses wrapped in PVC films with the highest concentration found after 20 days storage. The PE cling-film was shown to possess a simpler VOC profile, lacking some molecules peculiar to PVC films. The same conclusions can be drawn for cheeses wrapped in the PE cling-film. Other VOCs found in wrapped cheeses were likely to have been released either by direct transfer from the materials used for the manufacture of cling-films or from contamination of the films. Overall, HS-SPME is shown to be a rapid and solvent free technique to screen the VOCs profile of cling-films, and to detect VOCs migration from cling-films to cheese under real retail storage conditions.

  17. Simulation of melting in crystalline polyethylene

    NASA Astrophysics Data System (ADS)

    Zubova, E. A.; Balabaev, N. K.; Musienko, A. I.; Gusarova, E. B.; Mazo, M. A.; Manevitch, L. I.; Berlin, A. A.

    2012-06-01

    We carry out a molecular dynamics simulation of the first stages of constrained melting in crystalline polyethylene (PE). When heated, the crystal undergoes two structural phase transitions: from the orthorhombic (O) phase to the monoclinic (M) phase, and then to the columnar (C), quasi-hexagonal, phase. The M phase represents the tendency to the parallel packing of planes of PE zigzags, and the C phase proves to be some kind of oriented melt. We follow both the transitions O→M and M→C in real time and establish that, at their beginning, the crystal tries (and fails) to pass into the partially ordered phases similar to the RI and RII phases of linear alkanes, correspondingly. We discuss the molecular mechanisms and driving forces of the observed transitions, as well as the reasons why the M and C phases in PE crystals substitute for the rotator phases in linear alkanes.

  18. Degradable polyethylene: fantasy or reality.

    PubMed

    Roy, Prasun K; Hakkarainen, Minna; Varma, Indra K; Albertsson, Ann-Christine

    2011-05-15

    Plastic waste disposal is one of the serious environmental issues being tackled by our society today. Polyethylene, particularly in packaging films, has received criticism as it tends to accumulate over a period of time, leaving behind an undesirable visual footprint. Degradable polyethylene, which would enter the eco-cycle harmlessly through biodegradation would be a desirable solution to this problem. However, the "degradable polyethylene" which is presently being promoted as an environmentally friendly alternative to the nondegradable counterpart, does not seem to meet this criterion. This article reviews the state of the art on the aspect of degradability of polyethylene containing pro-oxidants, and more importantly the effect these polymers could have on the environment in the long run. On exposure to heat, light, and oxygen, these polymers disintegrate into small fragments, thereby reducing or increasing the visual presence. However, these fragments can remain in the environment for prolonged time periods. This article also outlines important questions, particularly in terms of time scale of complete degradation, environmental fate of the polymer residues, and possible accumulation of toxins, the answers to which need to be established prior to accepting these polymers as environmentally benign alternatives to their nondegradable equivalents. It appears from the existing literature that our search for biodegradable polyethylene has not yet been realized.

  19. Structure-property relationship in polyethylene reinforced by polyethylene-grafted multi-walled carbon nanotubes.

    PubMed

    Causin, Valerio; Yang, Bing-Xing; Marega, Carla; Goh, Suat Hong; Marigo, Antonio

    2008-04-01

    Polyethylene-grafted multiwalled carbon nanotubes (PE-g-MWNT) were used to reinforce polyethylene (PE). The nanocomposites possessed not only improved stiffness and strength, but also increased ductility and toughness. The effects on the structure and morphology of composites due to pristine multiwalled carbon nanotubes (MWNT) and PE-g-MWNT were studied and compared using small angle X-ray scattering (SAXS), wide angle X-ray diffraction (WAXD) and differential scanning calorimetry (DSC). The SAXS long period, crystalline layer thickness and crystallinity of polymer lamellar stacks were found to decrease significantly in MWNT composites, while the decreases were much smaller in PE-g-MWNT composites. PE-g-MWNT allowed a more efficient and unhindered crystallization at a lamellar level, while MWNT disrupted the order of lamellar stacks, probably because of their tendency to aggregate. The SAXS crystallinity and the mechanical properties of the composites showed similar trends as a function of MWNT content. This suggested that the improvement of the interfacial strength between polymer and carbon nanotubes was a result of synergistic effects of better dispersion of the filler, better stress transfer, due to the grafting of polymer and MWNT, and the nucleation of a crystalline phase around MWNT. The latter effect was confirmed by measurements of kinetics of non-isothermal crystallization.

  20. MARTINI Coarse-Grained Models of Polyethylene and Polypropylene.

    PubMed

    Panizon, Emanuele; Bochicchio, Davide; Monticelli, Luca; Rossi, Giulia

    2015-06-25

    The understanding of the interaction of nanoplastics with living organisms is crucial both to assess the health hazards of degraded plastics and to design functional polymer nanoparticles with biomedical applications. In this paper, we develop two coarse-grained models of everyday use polymers, polyethylene (PE) and polypropylene (PP), aimed at the study of the interaction of hydrophobic plastics with lipid membranes. The models are compatible with the popular MARTINI force field for lipids, and they are developed using both structural and thermodynamic properties as targets in the parametrization. The models are then validated by showing their reliability at reproducing structural properties of the polymers, both linear and branched, in dilute conditions, in the melt, and in a PE-PP blend. PE and PP radius of gyration is correctly reproduced in all conditions, while PE-PP interactions in the blend are slightly overestimated. Partitioning of PP and PE oligomers in phosphatidylcholine membranes as obtained at CG level reproduces well atomistic data.

  1. Structure-property relationships: Model studies on melt-extruded uniaxially-oriented high density polyethylene films having well defined morphologies

    NASA Astrophysics Data System (ADS)

    Zhou, Hongyi

    High density polyethylene (HDPE) films having simple and well-defined stacked lamellar morphology, either with or without a distinct presence of row-nucleated fibril structures, have been utilized as model materials to carry out investigations on solid state structure-property relationships. Mechanical tests, including tensile (INSTRON), creep (TMA), and dynamic mechanical (DMTA) tests, were performed at different angles with respect to the original machine direction (MD) of the melt extruded films; morphological changes as a result of these mechanical tests were detected by WAXS, SAXS, and TEM. Crystalline lamellar thickness and its distribution were determined by DSC, SAXS, TEM and AFM experiments. In the large strain deformation study (chapter 4.0), samples were stretched at 00sp°, 45sp° and 90sp° angles with respect to the original MD. A distinct orientation dependence of the tensile behavior was observed and correlated to the corresponding deformation modes and morphological changes, namely (1) lamellar separation and fragmentation by chain slip for the 00sp° stretch, (2) lamellar break-up via chain pull-out for the 90sp° stretch, and (3) lamellar shear, rotation and break-up through chain slip and/or tilt for the 45sp° stretch. A strong strengthening effect was observed for samples with row-nucleated fibril structures at the 00sp° stretch; whereas for the 90sp° stretch, the presence of such structures significantly limited deformability of the samples. In the dynamic strain mechanical alpha relaxation study (chapter 5.0), samples were tested at nine different angles with respect to the original MD, and the morphologies of samples before and after the dynamic tests were also investigated. The mechanical dispersions for the 00sp° and 90sp° tests were believed to arise essentially from the crystalline phase, and they contain contributions from two earlier recognized sub-relaxations of alphasbI and alphasbII. While for the 45sp° test, in addition to a

  2. Crosslinked blends and coextruded films by electron beam

    NASA Astrophysics Data System (ADS)

    Vallat, M. F.; Marouani, S.; Perraud, S.; Mendoza Patlan, N.

    2005-07-01

    Morphology, thermal and mechanical properties of polymer blends and coextruded films of hydrogenated copolymer of butadiene and acrylonitrile (HNBR) and polyethylene-co-octene (PE-co-O) are considered before and after electron beam crosslinking. It is known that the properties are depending not only on the crosslinks in the bulk of the polymers but also on that created in the interfacial domain. It is however very difficult to have direct evidence of the interfacial crosslinks. Moreover the two polymers are not compatible and the addition of an ethylene vinyl acetate copolymer as a potential polymer compatibiliser is considered.

  3. Polyhomologation based on in situ generated boron-thexyl-silaboracyclic initiating sites: a novel strategy towards the synthesis of polyethylene-based complex architectures.

    PubMed

    Zhang, Zhen; Zhang, Hefeng; Gnanou, Yves; Hadjichristidis, Nikos

    2015-06-21

    A novel strategy, based on the in situ generated boron-thexyl-silaboracyclic initiating sites for the polyhomologation of dimethylsulfoxonium methylide, has been developed for the synthesis of complex polyethylene-based architectures. As examples, the synthesis of a 4-arm polyethylene star, three (polystyrene)(polyethylene)2 3-miktoarm stars and a PE-branched double graft copolymer is given.

  4. Effects of Biomass in Polyethylene or Polylactic Acid Composites

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Previous studies have shown that compounding Polyethylene (PE) or Polylactic acid (PLA) with a dairy-based bioplastic resulted in composites with good mechanical properties. In this study, mass ratios of a dairy-protein-based material (DBP) ranging from 0, 5, 10 and 20 wt% replaced equivalent masse...

  5. Biocompatibility of modified ultra-high-molecular-weight polyethylene

    NASA Astrophysics Data System (ADS)

    Novotná, Z.; Lacmanová, V.; Rimpelová, S.; Juřik, P.; Polívková, M.; Å vorčik, V.

    2016-09-01

    Ultra-high-molecular-weight polyethylene (UHMWPE, PE) is a synthetic polymer used for biomedical applications because of its high impact resistance, ductility and stability in contact with physiological fluids. Therefore this material is being used in human orthopedic implants such as total joint replacements. Surface modification of this material relates to changes of its surface hydrophilicity, energy, microstructure, roughness, and morphology, all influencing its biological response. In our recent work, PE was treated by an Ar+ plasma discharge and then grafted with biologically active polyethylene glycol in order to enhance adhesion and proliferation of mouse fibroblast (L929). The surface properties of pristine PE and its grafted counterparts were studied by goniometry (surface wettability). Furthermore, Atomic Force Microscopy was used to determine the surface morphology and roughness. The biological response of the L929 cell lines seeded on untreated and plasma treated PE matrices was quantified in terms of the cell adhesion, density, and metabolic activity. Plasma treatment leads to the ablation of the polymer surface layers. Plasma treatment and subsequent poly(ethylene glycol) grafting lead to dramatic changes in the polymer surface morphology and roughness. Biological tests, performed in vitro, show increased adhesion and proliferation of cells on modified polymers. Grafting with poly(ethylene glycol) increases cell proliferation compared to plasma treatment.

  6. Effect of surface topography and morphology on space charge packets in polyethylene

    NASA Astrophysics Data System (ADS)

    Yuanxiang, Zhou; Yunshan, Wang; Ninghua, Wang; Qinghua, Sun

    2009-08-01

    Polyethylene (PE) is a major kind of internal insulating material. With great progresses of space charge measurement technologies in the last three decades, lots of researches are focused on space charge in PE. The heat pressing and annealing condition of polyethylene affect its morphology obviously. During the heat pressing, the surface of PE forms different surface topographies because of different substrate materials. Surface topography has great relation to the epitaxial crystallization layer and influences the space charge characteristic of PE dramatically. This paper studied the formation process of different surface topographies and their micrographic characters in low density polyethylene (LDPE). pulsed electro-acoustic (PEA) method was used to measure the space charge distribution of samples with different surface topographies and morphologies in LDPE. The effect of surface topography and morphology to space charge packet were studied. The surface topography has great influence on space charge packet polarity and morphology has influence on both movement speed rate and polarity of space charge packet.

  7. Combustion of PMMA, PE, and PS in a ramjet

    SciTech Connect

    van der Geld, C.W.M. ); Korting, P.A.O.G. ); Wijchers, T. )

    1990-03-01

    This paper reports the combustion behavior of polymethylmetharcrylate (PMMA), polyethylene (PE), and polystyrene (PS) with air investigated in a connected pipe test facility; spectroscopy showed the presence of OH, C{sub 2}, and CH and temperatures between 1300 and 3000 K during combustion. Particular attention was focused on regression rate and combustion efficiency and the role of temperature and soot production. The present investigation gives an understanding of the most important phenomena that control (or emanate from) the combustion of a cylindrical solid fuel with a rearward facing step, and this has application for solid fuel ramjets, the safe burning of toxic waste, and hot gas generators. The results are summarized.

  8. Tribological characteristics of polyethylene glycol (PEG) as a lubricant for wear resistance of ultra-high-molecular-weight polyethylene (UHMWPE ) in artificial knee join.

    PubMed

    Kobayashi, Masanori; Koide, Takayuki; Hyon, Suong-Hyu

    2014-10-01

    For the longevity of total knee joint prostheses, we have developed an artificial lubricant using polyethylene glycol (PEG) for the prevention of wear of ultra-high-molecular-weight polyethylene (UHMWPE). In the present study, the lubricative function of this PEG lubricant was evaluated by a wear test using Co-Cr alloy and UHMWPE counter surface samples. As a result, human synovial fluid including the PEG lubricant showed good result regarding the wear volume and a worn surface of UHMWPE. Considering its lubrication mechanism, it is suspected that interaction between the PEG molecules and the proteins in synovial fluid was involved. Since PE molecules are also organic compounds having a hydroxyl group at one or both ends, the albumin and PEG molecule complex would have bound more strongly to the metal oxide surface and UHMWPE surfaces might enhance and stabilize the lubricating film between the contact surfaces under the boundary lubrication. This study suggests that PEG lubricant as an intra-articular viscous supplement has the potential to prevent wear of UHMWPE by mixing with synovial fluid and to contribute to the longevity of knee joint prostheses.

  9. Cell adhesion and proliferation on polyethylene grafted with Au nanoparticles

    NASA Astrophysics Data System (ADS)

    Kasálková, N. Slepičková; Slepička, P.; Kolská, Z.; Sajdl, P.; Bačáková, L.; Rimpelová, S.; Švorčík, V.

    2012-02-01

    Plasma treatment and subsequent Au nano-particles grafting of polyethylene (PE) lead to changes in surface morphology, roughness and wettability, significantly increasing the attractiveness of the material for cells. The PE samples were exposed to argon plasma. Plasma modified PE was chemically grafted by immersion to biphenyldithiol and consequently into solution of Au nano-particles. Changes in chemical structure of the modified PE were studied using X-ray Photoelectron Spectroscopy (XPS) and electrokinetic analysis ( ζ-potential). The surface wettability of the modified PE samples was examined by measurement of the contact angle by standard goniometry. The surface morphology of the plasma modified PE and that grafted with Au nano-particles was studied by Atomic Force Microscopy (AFM). The modified PE samples were seeded with rat vascular smooth muscle cells (VSMCs) and their adhesion and proliferation were studied. Chemically bounded biphenyldithiol increases the number of the incorporated gold nano-particles and changes sample surface properties. The presence of the biphenyldithiol and the gold nano-particles on the PE surface influences dramatically adhesion and proliferation of VSMCs.

  10. Grafting functional antioxidants on highly crosslinked polyethylene

    NASA Astrophysics Data System (ADS)

    Al-Malaika, S.; Riasat, S.; Lewucha, C.

    2016-05-01

    The problem of interference of antioxidants, such as hindered phenols, with peroxide-initiated crosslinking of polyethylene was addressed through the use of functional (reactive) graftable antioxidants (g-AO). Reactive derivatives of hindered phenol and hindered amine antioxidants were synthesised, characterised and used to investigate their grafting reactions in high density polyethylene; both non-crosslinked (PE) and highly peroxide-crosslinked (PEXa). Assessment of the extent of in-situ grafting of the antioxidants, their retention after exhaustive solvent extraction in PE and PEXa, and the stabilising performance of the grafted antioxidants (g-AO) in the polymer were examined and benchmarked against conventionally stabilised crosslinked & non-crosslinked polyethylene. It was shown that the functional antioxidants graft to a high extent in PEXa, and that the level of interference of the g-AOs with the polymer crosslinking process was minimal compared to that of conventional antioxidants which bear the same antioxidant function. The much higher level of retention of the g-AOs in PEXa after exhaustive solvent extraction, compared to that of the corresponding conventional antioxidants, accounts for their superior long-term thermal stabilising performance under severe extractive conditions.

  11. Waste product profile: Polyethylene terephthalate

    SciTech Connect

    Miller, C.

    1996-02-01

    Polyethylene terephthalate (PET) is a plastic resin used primarily to make bottles. Soft drinks are the primary product packaged in PET. Salad dressing, peanut butter, and other household and consumer products also use PET bottles. PET is also used for film, sheeting for cups and food trays, ovenable trays, and other uses. PET is a relatively new packaging resin, first commercialized in the early `70s. Because it is an ``engineered`` resin, it is more expensive than commodity resins such as high-density polyethylene (HDPE). The primary market for recycled PET is the fiber industry, which uses PET for carpet fiber, sweaters and other clothing, and for other uses. Recycled PET can also be used for food and beverage containers. Export markets, particularly Asian countries, are becoming increasingly important.

  12. Radiative human body cooling by nanoporous polyethylene textile

    NASA Astrophysics Data System (ADS)

    Hsu, Po-Chun; Song, Alex Y.; Catrysse, Peter B.; Liu, Chong; Peng, Yucan; Xie, Jin; Fan, Shanhui; Cui, Yi

    2016-09-01

    Thermal management through personal heating and cooling is a strategy by which to expand indoor temperature setpoint range for large energy saving. We show that nanoporous polyethylene (nanoPE) is transparent to mid-infrared human body radiation but opaque to visible light because of the pore size distribution (50 to 1000 nanometers). We processed the material to develop a textile that promotes effective radiative cooling while still having sufficient air permeability, water-wicking rate, and mechanical strength for wearability. We developed a device to simulate skin temperature that shows temperatures 2.7° and 2.0°C lower when covered with nanoPE cloth and with processed nanoPE cloth, respectively, than when covered with cotton. Our processed nanoPE is an effective and scalable textile for personal thermal management.

  13. Radiative human body cooling by nanoporous polyethylene textile.

    PubMed

    Hsu, Po-Chun; Song, Alex Y; Catrysse, Peter B; Liu, Chong; Peng, Yucan; Xie, Jin; Fan, Shanhui; Cui, Yi

    2016-09-02

    Thermal management through personal heating and cooling is a strategy by which to expand indoor temperature setpoint range for large energy saving. We show that nanoporous polyethylene (nanoPE) is transparent to mid-infrared human body radiation but opaque to visible light because of the pore size distribution (50 to 1000 nanometers). We processed the material to develop a textile that promotes effective radiative cooling while still having sufficient air permeability, water-wicking rate, and mechanical strength for wearability. We developed a device to simulate skin temperature that shows temperatures 2.7° and 2.0°C lower when covered with nanoPE cloth and with processed nanoPE cloth, respectively, than when covered with cotton. Our processed nanoPE is an effective and scalable textile for personal thermal management.

  14. Preparation of Polyethylene Composites Containing Silver(I) Acylpyrazolonato Additives and SAR Investigation of their Antibacterial Activity.

    PubMed

    Marchetti, Fabio; Palmucci, Jessica; Pettinari, Claudio; Pettinari, Riccardo; Marangoni, Mirko; Ferraro, Stefano; Giovannetti, Rita; Scuri, Stefania; Grappasonni, Iolanda; Cocchioni, Mario; Maldonado Hodar, Francisco José; Gunnella, Roberto

    2016-11-02

    Novel composite materials PEn (n = 1-9) have been prepared by an easily up-scalable embedding procedure of three different families of Ag(I) acylpyrazolonato complexes in polyethylene (PE) matrix. In details, PE1-PE3 composites contain polynuclear [Ag(Q(R))]n complexes, PE4-PE6 contain mononuclear [Ag(Q(R))(L)m] complexes and PE7-PE9 are loaded with mononuclear [Ag(Q(R)) (PPh3)2] complexes, respectively (where L = 1-methylimidazole or 2-ethylimidazole, m = 1 or 2, and HQ(R) = 1-phenyl-3-methyl-4-RC(═O)-5-pyrazolone, where in detail HQ(fb), R = -CF2CF2CF3; HQ(cy), R = -cyclo-C6H11; HQ(be), R = -C(H)═C(CH3)2). The PEn composites, prepared by using a 1:1000 w/w silver additive/polyethylene ratio, have been characterized in bulk by IR spectroscopy and TGA analyses, which confirmed that the properties of polyethylene matrix are essentially unchanged. AFM, SEM, and EDX surface techniques show that silver additives form agglomerates with dimensions 10-100 μm on the polyethylene surface, with a slight increment of surface roughness of pristine plastic within 50 nm. However, the elastic properties of the composites are essentially the same of PE. The antibacterial activity of all composites has been tested against three bacterial strains (E. coli, P. aeruginosa and S. aureus) and results show that two classes of composites, PE1-PE3 and PE4-PE6, display high and persistent bactericidal and bacteriostatic activity, comparable to PE embedded with AgNO3. By contrast, composites PE7-PE9 exhibit a reduced antibacterial action. Contact and release tests in several conditions for specific migration of Ag(+) from plastics, indicate a very limited but time persistent release of silver ions from PE1-PE6 composites, thus suggesting that they are potential antibacterial materials for future applications. Instead, PE7-PE9 almost do not release silver, only trace levels of silver ions being detected, in accordance with their reduced antibacterial action. None of the composites is

  15. Li + grafting of ion irradiated polyethylene

    NASA Astrophysics Data System (ADS)

    Švorčík, V.; Rybka, V.; Vacík, J.; Hnatowicz, V.; Öchsner, R.; Ryssel, H.

    1999-02-01

    Foils of oriented polyethylene (PE) were irradiated with 63 keV Ar + and 155 keV Xe + ions to different fluences at room temperature and then doped from water solution of LiCl. The as irradiated and irradiated plus doped samples were examined by IR, EPR and neutron depth profiling (NDP) technique. The sheet resistance was also measured by the standard two points method. After Li salt doping of ion modified layer of PE, a reaction between degraded macromolecules and Li occur and thus a new chemical structure C-Li + is formed. Owing to the presence of these cations on the polymer chain, the irradiated plus doped layer exhibits higher electric conductivity compared to as-irradiated ones.

  16. Water film thickness-dependent conformation and diffusion of single-strand DNA on poly(ethylene glycol)-silane surface

    PubMed Central

    Park, Jae Hyun; Aluru, N. R.

    2010-01-01

    In this paper, we investigate, using molecular dynamics simulations, the conformation and diffusion of longer and shorter single-strand DNA (ssDNA) as a function of water film thickness. While the conformation of the shorter ssDNA is significantly affected and the diffusion is suppressed with reduction in water film thickness, the conformation and diffusion of the longer DNA is not influenced. We explain our observations by considering the competition between stacking interaction of bases and solvation tendency of ssDNA. This paper suggests an approach to control the surface motion of ssDNA in nanoscale water films using film thickness. PMID:20404938

  17. Molecular dynamics of polymer crystallization revisited: Crystallization from the melt and the glass in longer polyethylene

    NASA Astrophysics Data System (ADS)

    Yamamoto, Takashi

    2013-08-01

    Molecular mechanisms of the steady-state growth of the chain folded lamella and the cold crystallization across the glass transition temperature Tg are investigated by molecular dynamics simulation for a system of long polyethylene (PE)-like polymers made of 512 united atoms C512. The present paper aims to reconsider results of our previous simulations for short PE-like polymers C100 by carrying out very long simulations up to 1 μs for more realistic systems of much longer chains, thereby to establish the firm molecular image of chain-folded crystallization and clarify the specific molecular process of cold crystallization. We observe that the chain-folded lamella shows fast thickening-growth keeping marked tapered growth front. Despite the fast growth in much longer chains, the fold-surface is found to be predominantly of adjacent-reentry. Detailed inspections of the molecular pathway give an insightful image that can explain the apparently contradicting results. In addition, the fold-structure with specific spatial heterogeneity is found to give rise to heterogeneous mobility within the crystalline region. On the other hand, investigations of the cold crystallization during slow heating of the glassy film across Tg is found to give a granular texture made of small crystallites. The crystallites are found to nucleate preferentially near the free surfaces having lower Tg, and to be dominantly edge-on showing a definite tendency to orient their chain axes parallel to the free surface.

  18. Biomimetic hydration lubrication with various polyelectrolyte layers on cross-linked polyethylene orthopedic bearing materials.

    PubMed

    Kyomoto, Masayuki; Moro, Toru; Saiga, Kenichi; Hashimoto, Masami; Ito, Hideya; Kawaguchi, Hiroshi; Takatori, Yoshio; Ishihara, Kazuhiko

    2012-06-01

    Natural joints rely on fluid thin-film lubrication by the hydrated polyelectrolyte layer of cartilage. However, current artificial joints with polyethylene (PE) surfaces have considerably less efficient lubrication and thus much greater wear, leading to osteolysis and aseptic loosening. This is considered a common factor limiting prosthetic longevity in total hip arthroplasty (THA). However, such wear could be mitigated by surface modification to mimic the role of cartilage. Here we report the development of nanometer-scale hydrophilic layers with varying charge (nonionic, cationic, anionic, or zwitterionic) on cross-linked PE (CLPE) surfaces, which could fully mimic the hydrophilicity and lubricity of the natural joint surface. We present evidence to support two lubrication mechanisms: the primary mechanism is due to the high level of hydration in the grafted layer, where water molecules act as very efficient lubricants; and the secondary mechanism is repulsion of protein molecules and positively charged inorganic ions by the grafted polyelectrolyte layer. Thus, such nanometer-scaled hydrophilic polymers or polyelectrolyte layers on the CLPE surface of acetabular cup bearings could confer high durability to THA prosthetics.

  19. The New P.E.

    ERIC Educational Resources Information Center

    Vandertie, Joan; Corner, Amy B.; Corner, Kevin J.

    2012-01-01

    Marana Middle School in Tucson, Ariz., scrapped its traditional P.E. program that emphasized team sports and shifted to a program that focuses on lifetime fitness, student choice in activities, and nutrition and health education. The program also includes student leadership development and informal community service. As a result, Marana students…

  20. Charge distribution and conduction characteristics of 2-vinylpyridine-grafted polyethylenes

    NASA Astrophysics Data System (ADS)

    Suh, Kwang S.; Kim, Jong Eun; Oh, Woo Jung; Yoon, Ho Gyu; Takada, Tatsuo

    2000-05-01

    This article describes electrical properties such as space charge distribution and electrical conduction characteristics of 2-vinylpyridine (VP) grafted low density polyethylenes (PE). The VP incorporated onto PE chains changes electrical properties of PE. For example, the homocharge found in virgin PE decreases with the increase of graft ratio. As a result of the nitrogen acting as an electron donor, no space charge develops at high graft ratios. It has been found that VP reduces the current density in PE. Grafted PE with VP content of 0.754 wt % has also been found to obey a space charge limited conduction mechanism: effective charge mobility at 70 °C was calculated to be 4.6×10-16 m2/V s: an activation energy for the conduction was estimated to be 0.81 eV at 70 °C.

  1. Modeling uptake of hydrophobic organic contaminants into polyethylene passive samplers.

    PubMed

    Thompson, Jay M; Hsieh, Ching-Hong; Luthy, Richard G

    2015-02-17

    Single-phase passive samplers are gaining acceptance as a method to measure hydrophobic organic contaminant (HOC) concentration in water. Although the relationship between the HOC concentration in water and passive sampler is linear at equilibrium, mass transfer models are needed for nonequilibrium conditions. We report measurements of organochlorine pesticide diffusion and partition coefficients with respect to polyethylene (PE), and present a Fickian approach to modeling HOC uptake by PE in aqueous systems. The model is an analytic solution to Fick's second law applied through an aqueous diffusive boundary layer and a polyethylene layer. Comparisons of the model with existing methods indicate agreement at appropriate boundary conditions. Laboratory release experiments on the organochlorine pesticides DDT, DDE, DDD, and chlordane in well-mixed slurries support the model's applicability to aqueous systems. In general, the advantage of the model is its application in the cases of well-agitated systems, low values of polyethylene-water partioning coefficients, thick polyethylene relative to the boundary layer thickness, and/or short exposure times. Another significant advantage is the ability to estimate, or at least bound, the needed exposure time to reach a desired CPE without empirical model inputs. A further finding of this work is that polyethylene diffusivity does not vary by transport direction through the sampler thickness.

  2. Determinants of PE Teachers Career Intentions

    ERIC Educational Resources Information Center

    Mäkelä, Kasper; Hirvensalo, Mirja; Whipp, Peter R.

    2015-01-01

    One of the cause's célèbre in the field of education has been teacher attrition; Physical education (PE) is no different. Some PE teachers are leaving the profession because they encounter stress and dissatisfaction in their profession. The purpose of this study is to determine the aspects that keep PE teachers happy and remaining in the…

  3. Enhancement of adhesion by a transition layer: Deposition of a-C film on ultrahigh molecular weight polyethylene (UHMWPE) by magnetron sputtering

    NASA Astrophysics Data System (ADS)

    He, F. F.; Bai, W. Q.; Li, L. L.; Wang, X. L.; Xie, Y. J.; Jin, G.; Tu, J. P.

    2016-02-01

    An amorphous carbon (a-C) film is deposited on the plasma-treated UHMWPE substrate using a closed field unbalanced magnetron sputtering to improve its tribological properties. During the plasma treatment period, a transition layer is prepared by high energy ion bombardment at a bias voltage of -500 V to enhance the adhesion between the a-C film and the substrate. The mechanical and tribological properties of the a-C film were evaluated by nano-indentation and ball-on-disk tribometer. After deposition of a-C film with a thickness 900 nm, the nano-hardness of UHMWPE significantly increases from 47 MPa to 720 MPa and the wear rate decreases from 9.82 × 10-15 m3 N-1 m-1 to 4.78 × 10-15 m3 N-1 m-1 in bovine calf serum solution. The formation of the transition layer is believed to be the reason why the vertical adhesion between the a-C film and the UHMWPE substrate is enhanced.

  4. Preparation of extruded polyethylene/chitosan blends compatibilized with polyethylene-graft-maleic anhydride.

    PubMed

    Quiroz-Castillo, J M; Rodríguez-Félix, D E; Grijalva-Monteverde, H; Del Castillo-Castro, T; Plascencia-Jatomea, M; Rodríguez-Félix, F; Herrera-Franco, P J

    2014-01-30

    Novel films of polyethylene and chitosan were obtained using extrusion. These polymers have interesting properties, and processing them with methods that are of high use in the industry, such as the extrusion method, can have a significant effect on the potential applications of these materials. The individual materials were thermally characterized; after this, extruded films of low density polyethylene and chitosan mixtures were prepared with the addition of polyethylene-graft-maleic anhydride as a compatibilizer for the blends, and glycerol, as a plasticizer for chitosan. The use of compatibilizer and plasticizer agents improved the processability and compatibility of the mixtures, as well as their mechanical properties, as revealed by mechanical property measurements and scanning electron microscopy. It was possible to prepare blends with a maximum chitosan content of 20 wt%. The material stiffness increased with the increase of chitosan in the sample. FTIR studies revealed the existence of an interaction between the compatibilizer and chitosan.

  5. EFFECTS OF TRITIUM ON UHMW-PE, PTFE, AND VESPEL POLYIMIDE

    SciTech Connect

    Clark, E; Kirk Shanahan, K

    2006-11-01

    Samples of ultrahigh molecular weight polyethylene (UHMW-PE), polytetrafluoroethylene (PTFE), and the polyimide Vespel{reg_sign} were exposed to tritium gas in closed containers initially at 101 kPa (1 atmosphere) pressure and ambient temperature for various times up to 2.3 years. Tritium exposure effects on the samples were characterized by dynamic mechanical analysis (DMA) and radiolysis products were characterized by measuring the total final pressure and composition in the exposure containers at the end of exposure period.

  6. Effect of the precise branching of polyethylene at each 21st CH2 group on its phase transitions, crystal structure, and morphology

    SciTech Connect

    Qui, Wulin; Sworen, John; Pyda, Marek {nmn}; Nowak-Pyda, Elisabieta; Habenschuss, Anton {Tony}; Wagener, Kenneth; Wunderlich, Bernhard {nmn}

    2006-01-01

    Three linear polyethylenes with branches at every 21st backbone atom have been analyzed by differential scanning calorimetry (DSC) and quasi-isothermal, temperature-modulated DSC. The branches were methyl (PE1M), dimethyl (PE2M), and ethyl groups (PE1E). Linear polyethylene (HDPE) and atactic poly(octadecyl acrylate) (PODA) were also analyzed. All were compared to a random poly(ethylene-co-octene-1) of similar branch concentration (LLDPE) and poly(4,4'-phthaloimidobenzoyldoeicosyleneoxycarbonyl) (PEIM-22). The HDPE has the highest melting temperature and crystallinity with relatively large contributions of reversing melting when grown as folded-chain crystals. The precisely branched polyethylenes and copolymers have lower melting temperatures and heats of fusion. Of the branched samples, PE1M crystallizes more readily, followed by PE1E and PE2M, with PE2M showing cold crystallization. In contrast to paraffins of equal length which melt fully reversibly, the precisely designed, branched polymers melt largely irreversibly with small amounts of reversing melting, which is least for the best-grown crystals. The PE1M forms monoclinic, PE1E, pseudohexagonal, or triclinic crystals, and PE2M has a multitude of crystal structures.

  7. Improved self-healing of polyethylene/carbon black nanocomposites by their shape memory effect.

    PubMed

    Wang, Xiaoyan; Zhao, Jun; Chen, Min; Ma, Lan; Zhao, Xiaodong; Dang, Zhi-Min; Wang, Zhenwen

    2013-02-07

    In this work, the improved self-healing of cross-linked polyethylene (PE) (cPE)/carbon black (CB) nanocomposites by their shape memory effect (SME) is investigated. CB nanoparticles are found to be homogeneously dispersed in the PE matrix and significantly increase the strength of the materials. Compared with the breaking of linear PE (lPE) at the melting temperature (T(m)), the cPE and cPE/CB nanocomposites still have high strength above T(m) due to the formation of networks. The cPE and cPE/CB nanocomposites show both high strain fixity ratio (R(f)) and high strain recovery ratio (R(r)). Crystallization-induced elongation is observed for all the prepared shape memory polymer (SMP) materials and the effect becomes less remarkable with increasing volume fraction of CB nanoparticles (v(CB)). The scratch self-healing tests show that the cross-linking of PE matrix, the addition of CB nanoparticles, and the previous stretching in the direction perpendicular to the scratch favor the closure of the scratch and its complete healing. This SME-aided self-healing could have potential applications in diverse fields such as coating and structure materials.

  8. Direction of polyethylene separator development for the SLI market

    SciTech Connect

    Navarrete, J.

    1997-12-01

    Recent separator advancements have improved the oxidation stability and puncture resistance of Polyethylene (PE) separators. These improvements, at the same time, have been accomplished even as the market continues to demand separators with lower backweb thickness. Results of development work to evaluate improved oxidation resistance is presented. Evaluation of separator characteristics as well as separator performance in a battery are presented and form the basis for an improved separator design.

  9. Biodegradation of poly(hydroxy butanoic acid) copolymer mulch films in soil

    NASA Astrophysics Data System (ADS)

    Kukade, Pranav

    Agricultural mulch films that are used to cover soil of crop rows contribute to earlier maturation of crops and higher yield. Incineration and landfill disposals are the most common means of disposal of the incumbent polyethylene (PE) mulch films; however, these are not environment friendly options. Biodegradable mulch films that can be rototilled into the soil after crop harvest are a promising alternative to offset problems such as landfill disposal, film retrieval and disposal costs. In this study, an in-house laboratory scale test method was developed in which the rate of disintegration, as a result of biodegradation of films based on polyhydroxybutanoic acid (PHB) copolymers was investigated in a soil environment using the residual weight loss method. The influence of soil composition, moisture levels in the soil, and industry-standard anti-microbial additive in the film composition on the rate of disintegration of PHB copolymer films was investigated. The soil composition has significant effect on the disintegration kinetics of PHB copolymer films, since the increasing compost levels in the soil lowered the rate of disintegration of the film. Also, with the increase in moisture level up to a threshold limit, the microbial activity and, hence, the rate of disintegration increased. Lastly, the developed lab-scale test protocol was found to be sensitive to even small concentrations of industry-standard antimicrobial additive in the film composition.

  10. Migration of wear debris of polyethylene depends on bone microarchitecture.

    PubMed

    Libouban, Hélène; Massin, Philippe; Gaudin, Christine; Mercier, Philippe; Baslé, Michel F; Chappard, Daniel

    2009-08-01

    The mechanism of hip arthroplasties loosening is related to the migration of wear debris throughout the implant environment. In vivo, polyethylene particles (PE) were shown to infiltrate the bone implant interface and the medullary spaces of the cancellous bone. Our test hypothesis was that polyethylene particle migration is correlated to bone porosity. Bone samples with a high or low trabecular volume and microarchitecture were harvested in 20 calves and 20 human cadavers. They were extensively washed to remove marrow cells. Bone cylinders were filled with a light-curing monomer having the same viscosity as bone marrow. PE particles (7 and 33 microm) were deposited at the surface of the polymer. The bone cylinders were agitated during 7 days on an orbital shaker and the gel was left to polymerize at day light. X-ray microtomography was performed to characterize bone volume and microarchitecture. Cylinders were sectioned and observed under polarized light. The migration distance and rate were determined. Migration of PE particles strongly depended on trabecular bone volume and microarchitecture. We found a linear relationship (r = 0.61) between speed migration and bone volume and an exponential relationship between speed migration and bone architecture. The present in vitro model confirmed our hypothesis about the key role of bone microarchitecture in the migration of large PE wear particles. This is an explanation for the development of inflammatory reaction at distance from a prosthesis although our study did not include submicron particles.

  11. High-resolution poly(ethylene terephthalate) (PET) hot embossing at low temperature: thermal, mechanical, and optical analysis of nanopatterned films.

    PubMed

    Cecchini, Marco; Signori, Francesca; Pingue, Pasqualantonio; Bronco, Simona; Ciardelli, Francesco; Beltram, Fabio

    2008-11-04

    In this work we present controlled, low-damage nanotopographic surface modification of poly(ethylene terephthalate) (PET). High-resolution nanopatterning over macroscopic areas was performed by " low-temperature" hot embossing lithography (HEL). While for standard HEL the temperature is typically raised up to many tens of Celsius degrees above the polymer glass transition temperature (Tg), we demonstrate optimal results at a temperature very close to the bulk Tg of PET (72 degrees C). Nanopits and nanobarcodes were transferred onto the surface of PET commercial sheets, demonstrating reliable sub-100 nm resolution over macroscopic areas. Sample optical, mechanical, and thermal characteristics were systematically analyzed before and after embossing at low (75 degrees C) and high (150 degrees C) temperature by attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy, tensile tests, and differential scanning calorimetry (DSC). We show that, while conventional high-temperature HEL can lead to dramatic degradation of the polymer in terms of transparency, flexibility, and crystallinity content, our low-temperature process fully maintains original surface and bulk substrate properties.

  12. Conducting polymer films fabricated by oxidative graft copolymerization of aniline on poly(acrylic acid) grafted poly(ethylene terephthalate) surfaces.

    PubMed

    Wang, Jiku; Liu, Xuyan; Choi, Ho-Suk; Kim, Jong-Hoon

    2008-11-27

    A conductive polyaniline/poly(ethylene terephthalate) (PANI/PET) composite film was fabricated via the oxidative graft copolymerization of aniline (ANI) onto the plasma-induced poly(acrylic acid) (PAAc) grafted PET surface. The attenuated total reflectance Fourier transform infrared spectroscopy spectra (ATR-FTIR) and X-ray photoelectron spectroscopy (XPS) results confirmed that PANI was successfully grafted onto the surface of the PAAc-g-PET films. The effects of the experimental conditions on the percentage of PANI grafted onto the PAAc-g-PET films were extensively investigated. A very high grafting percentage of ANI can be obtained through the acid-base reaction between the aniline monomer and PAAc on the PAAc-g-PET surface at high temperature. As a result, the grafting percentage of PANI can be increased to as high as 12.18 wt %, which causes the surface resistance of the PANI-g-PAAc-g-PET film to be reduced to about 1000 Omega/sq. We predicted that this is because of the high flexibility of the PAAc molecular chains and high solubility of aniline, both of which facilitate the binding of aniline to PAAc during this high temperature acid-base reaction. It was observed by atomic force microscopy (AFM) that the PANI-modified PET surface exhibits higher size irregularity and surface roughness, which further indicated that a much greater number of aniline molecules can be reactively bonded to and distributed along the grafted AAc chains and that the PANI-g-PAAc-g-PET surface resulting from the sequential oxidative graft copolymerization can possess higher electrical conductivity.

  13. Transferability and Adhesion of Sol-Gel-Derived Crystalline TiO2 Thin Films to Different Types of Plastic Substrates.

    PubMed

    Amano, Natsumi; Takahashi, Mitsuru; Uchiyama, Hiroaki; Kozuka, Hiromitsu

    2017-01-31

    Anatase thin films were prepared on various plastic substrates by our recently developed sol-gel transfer technique. Polycarbonate (PC), poly(methyl methacrylate) (PMMA), polyethylene terephthalate (PET), polyethylene (PE), polypropylene (PP), polyether ether ketone (PEEK), and polyvinylidene chloride (PVDC) were employed as plastic substrates. A Si(100) substrate was first coated with a polyimide (PI)/polyvinylpyrrolidone (PVP) mixture layer, and an alkoxide-derived titania gel film was deposited on it by spin-coating. The resulting titania gel film was heated to 600 °C, during which the PI/PVP layer decomposed and the gel film was converted into a 60 nm thick anatase film. The anatase film was then transferred from the Si(100) substrate to the plastic substrate. This was achieved by heating the plastic/anatase/Si(100) stack in a near-infrared image furnace to 120-350 °C, depending on the type of plastic substrate, under unidirectional pressure. The anatase film cracked during transfer to PE, PP, PEEK, and PVDC substrates but did not crack during transfer to PC, PMMA, and PET substrates. The fraction of the total film area that was successfully transferred was assessed with the aid of image analysis. This fraction tended to be large for plastics with C═O and C-O groups and small for those without these groups. The film/substrate adhesion assessed by cross-cut tape tests also tended to be high for plastics with C═O and C-O groups and low for those without these groups. The adhesion to plastics without C═O or C-O groups could be enhanced and their transfer area fraction increased by oxidizing the native plastic surface by ultraviolet-ozone treatment prior to transfer.

  14. Plasma Treatment of Polyethylene Powder Particles in Hollow Cathode Glow Discharge

    SciTech Connect

    Wolter, Matthias; Quitzau, Meike; Bornholdt, Sven; Kersten, Holger

    2008-09-07

    Polyethylen (PE) is widely used in the production of foils, insulators, packaging materials, plastic bottles etc. Untreated PE is hydrophobic due to its unpolar surface. Therefore, it is hard to print or glue PE and the surface has to be modified before converting.In the present experiments a hollow cathode glow discharge is used as plasma source which is mounted in a spiral conveyor in order to ensure a combines transport of PE powder particles. With this set-up a homogeneous surface treatment of the powder is possible while passing the glow discharge. The plasma treatment causes a remarkable enhancement of the hydrophilicity of the PE powder which can be verified by contact angle measurements and X-ray photoelectron spectroscopy.

  15. An Investigation into Reducing Time Dependent Creep of a Polyethylene Geotextile using Glass Fiber Yarns

    NASA Astrophysics Data System (ADS)

    Xiong, Jun

    An investigation has been carried out to reduce the deformation behavior of polyethylene (PE) woven geotextile fabric by making PE fabric-glass yarn composite structure using stitching and laminating. The results showed that reinforcement significantly reduced the creep and IED as long as the tensile stress is lower than the total load bearing capacity of the glass yarns in the composite structure. However, the strength of PE-glass composite fabric was solely dependent on the strength of the glass yarns. The strength from PE yarns only contributes when all glass yarns are broken. Cast result of concrete columns using the glass yarn reinforced PE fabric by stitching method suggested that the glass yarn must face outside of the fabric formwork to avoid damage of both fabric surface and column surface.

  16. Nanocomposites polyethylene/argile destines a des applications electriques: Conception et relations structure-proprietes

    NASA Astrophysics Data System (ADS)

    Zazoum, Bouchaib

    The aim of this work is the manufacturing of PE/clay nanocomposites and to study the structure-property relationships of these materials. The nanocomposites materials were prepared by mixing a commercially available premixed LLDPE/O-MMT masterbatch into a polyethylene blend matrix containing 80 wt % low density polyethylene and 20 wt % high density polyethylene with and without anhydride modified polyethylene (PE-MA) as the compatibilizer using a co-rotating twin-screw extruder. Firstly, the effect of nanoclay and compatibilizer on the structure and dielectric response of PE/clay nanocomposites has been investigated. The microstructure of PE/clay nanocomposites was characterized by wide angle X-ray diffraction (WAXD) and scanning electron microscope (SEM). Thermal properties were examined by differential scanning calorimetry (DSC). The dielectric response of neat PE was compared with those of PE/clay nanocomposite with and without the compatibilizer in order to understand the effect of the quality of dispersion of nanoclay on dielectric response. In the nanocomposite materials two relaxation modes are detected in the dielectric losses. The first relaxation is due to a Maxwell-Wagner-Sillars interfacial polarization and the second relaxation is related to dipolar polarization. A relationship between the degree of dispersion and the relaxation rate f max of Maxwell-Wagner-Sillars was found and discussed. Secondly, PE/clay nanocomposites have been characterized by various techniques such as optical microscopy, AFM, TEM, TGA, DMTA and dielectric breakdown measurements. A correlation between structure and dielectric breakdown strength was discussed. Finally, a 3D simulation model by the finite element method is developed in order to study the effect of dispersion of nanoclay particles, varying the permittivity and radius of the inclusion on effective permittivity, electric field distribution and polarization. The simulation results were compared with theoretical

  17. [Biodegradation of polyethylene].

    PubMed

    Yang, Jun; Song, Yi-ling; Qin, Xiao-yan

    2007-05-01

    Plastic material is one of the most serious solid wastes pollution. More than 40 million tons of plastics produced each year are discarded into environment. Plastics accumulated in the environment is highly resistant to biodegradation and not be able to take part in substance recycle. To increase the biodegradation efficiency of plastics by different means is the main research direction. This article reviewed the recent research works of polyethylene biodegradation that included the modification and pretreatment of polyethylene, biodegradation pathway, the relevant microbes and enzymes and the changes of physical, chemical and biological properties after biodegradation. The study directions of exploiting the kinds of life-forms of biodegradation polyethylene except the microorganisms, isolating and cloning the key enzymes and gene that could produce active groups, and enhancing the study on polyethylene biodegradation without additive were proposed.

  18. Copper nanoparticles functionalized PE: Preparation, characterization and magnetic properties

    NASA Astrophysics Data System (ADS)

    Reznickova, A.; Orendac, M.; Kolska, Z.; Cizmar, E.; Dendisova, M.; Svorcik, V.

    2016-12-01

    We report grafting of copper nanoparticles (CuNP) on plasma activated high density polyethylene (HDPE) via dithiol interlayer pointing out to the structural and magnetic properties of those composites. The as-synthesized Cu nanoparticles have been characterized by high-resolution transmission electron microscopy (HRTEM/TEM) and UV-vis spectroscopy. Properties of pristine PE and their plasma treated counterparts were studied by different experimental techniques: X-ray photoelectron spectroscopy (XPS), UV-vis spectroscopy, energy dispersive X-ray spectroscopy (EDS), zeta potential, electron spin resonance (ESR) and SQUID magnetometry. From TEM and HRTEM analyses, it is found that the size of high purity Cu nanoparticles is (12.2 ± 5.2) nm. It was determined that in the CuNPs, the copper atoms are arranged mostly in the (111) and (200) planes. Absorption in UV-vis region by these nanoparticles is ranging from 570 to 670 nm. EDS revealed that after 1 h of grafting are Cu nanoparticles homogeneously distributed over the whole surface and after 24 h of grafting Cu nanoparticles tend to aggregate slightly. The combined investigation of magnetic properties using ESR spectrometry and SQUID magnetometry confirmed the presence of copper nanoparticles anchored on PE substrate and indicated ferromagnetic interactions.

  19. Functional separator consisted of polyimide nonwoven fabrics and polyethylene coating layer for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Shi, Chuan; Zhang, Peng; Huang, Shaohua; He, Xinyi; Yang, Pingting; Wu, Dezhi; Sun, Daoheng; Zhao, Jinbao

    2015-12-01

    In this paper, a composite membrane with nonwoven polyimide (PI) membrane as structural support and polyethylene (PE) particles coating layer as a thermal shutdown layer, is fabricated as the separator for lithium-ion battery. Different from PI nonwoven membrane, the PE coating PI nonwoven composite membrane (PE-PI-S) not only shows excellent thermal shutdown function, similar to traditional multilayer PP/PE/PP separator, but also exhibits much higher thermal stability, better wettability to the polar electrolyte and lower internal resistance than the PP/PE/PP separator. The electrolyte uptake and ionic conductivity of PE-PI-S increase from 58%, 0.84 mS cm-1 to 400%, 1.34 mS cm-1, respectively. Furthermore, the thermal shutdown function of PE-PI-S can be controlled widely in the temperature range from 120 °C to more than 200 °C while the multilayer PP/PE/PP separator only with a shutdown temperature range from 130 °C to 160 °C. Lithium ion battery with PE-PI-S nonwoven separator also shows excellent stable cycling and good rate performance.

  20. Diffusion of limonene in polyethylene.

    PubMed

    Limm, W; Begley, T H; Lickly, T; Hentges, S G

    2006-07-01

    Diffusion coefficients of limonene in various linear low-density polyethylene (LLDPE) and low-density polyethylene (LDPE) resins have been determined from sorption data using a thermogravimetric methodology. From these data, one can determine whether polymer synthesis parameters such as the choice of catalytic process or co-monomer result in substantial differences in how much food packaging additives might migrate to food. For example, LLDPE is currently manufactured using either one of two distinct catalytic processes: Ziegler-Natta (ZN) and metallocene, a single-site catalyst. ZN catalysis is a heterogeneous process that has dominated polyolefin synthesis over the last half-century. It involves a transition metal compound containing a metal-carbon bond that can handle repeated insertion of olefin units. In contrast, metallocene catalysis has fewer than 20 years of history, but has generated much interest due to its ability to produce highly stereospecific polymers at a very high yield. In addition to high stereospecificity, metallocene-catalysed polymers are significantly lower in polydispersity than traditional ZN counterparts. Absorption and desorption testing of heat-pressed films made from LLDPE and LDPE resins of varying processing parameters indicates that diffusion coefficients of limonene in these resins do not change substantially.

  1. Giant surfactants of poly(ethylene oxide)- b-polystyrene-(molecular nanoparticle): nanoparticle-driven self-assembly with sub-10-nm nanostructures in thin films

    NASA Astrophysics Data System (ADS)

    Hsu, Chih-Hao; Lin, Zhiwei; Dong, Xue-Hui; Hsieh, I.-Fan; Cheng, Stephen Z. D.

    2014-03-01

    Giant surfactants are built upon precisely attaching shape- and volume-persistent molecular nanoparticles (MNP) to polymeric flexible tails. The unique class of self-assembling materials, giant surfactants, has been demonstrated to form self-assembled ordered nanostructures, and their self-assembly behaviors are remarkably sensitive to primary chemical structures. In this work, two sets of giant surfactants with functionalized MNP attached to diblock copolymer tails were studied in thin films. Carboxylic acid-functionalized [60]fullerene (AC60) tethered with PEO- b-PS (PEO-PS-AC60) represents an ABA' (hydrophilic-hydrophobic-hydrophilic) giant surfactant, and fluoro-functionalized polyhedral oligomeric silsesquioxane (FPOSS) tethered with PEO- b-PS (PEO-PS-FPOSS) represents an ABC (hydrophilic-hydrophobic-omniphobic) one. The dissimilar chemical natures of the MNPs result in different arrangement of MNPs in self-assembled structures, the dispersion of AC60 in PEO domain and the single domain of FPOSS. Moreover, the chemically bonded MNPs could induce the originally disordered small molecular PEO- b-PS to form ordered cylindrical and lamellar structure, as evidenced by TEM and GISAXS, leading to sub-10-nm nanostructures of copolymer in the thin film state.

  2. Far-UV Annealed Inkjet-Printed In2O3 Semiconductor Layers for Thin-Film Transistors on a Flexible Polyethylene Naphthalate Substrate.

    PubMed

    Leppäniemi, Jaakko; Eiroma, Kim; Majumdar, Himadri; Alastalo, Ari

    2017-03-15

    The inkjet-printing process of precursor solutions containing In nitrate dissolved in 2-methoxyethanol is optimized using ethylene glycol as a cosolvent that allows the stabilization of the droplet formation, leading to a robust, repeatable printing process. The inkjet-printed precursor films are then converted to In2O3 semiconductors at flexible-substrate-compatible low temperatures (150-200 °C) using combined far-ultraviolet (FUV) exposure at ∼160 nm and thermal treatment. The compositional nature of the precursor-to-metal oxide conversion is studied using grazing incidence X-ray diffraction (GIXRD), X-ray reflectivity (XRR), and Fourier transform infrared (FTIR) spectroscopy that indicate that amorphous, high density (up to 5.87 g/cm(3)), and low impurity In2O3 films can be obtained using the combined annealing technique. Prolonged annealing (180 min) at 150 °C yields enhancement-mode TFTs with saturation mobility of 4.3 cm(2)/(Vs) and ∼1 cm(2)/(Vs) on rigid Si/SiO2 and flexible plastic PEN substrates, respectively. This paves the way for manufacturing relatively high-performance, printed metal-oxide TFT arrays on cheap, flexible substrate for commercial applications.

  3. Films.

    ERIC Educational Resources Information Center

    Philadelphia Board of Education, PA. Div. of Instructional Materials.

    The Affective Curriculum Research Project produced five films and two records during a series of experimental summer programs. The films and records form part of a curriculum designed to teach to the concerns of students. The films were an effort to describe the Philadelphia Cooperative Schools Program, to explain its importance, and to…

  4. Thermo-Gelation of Surface-Modified Polyethylene Microgels from Fragmentation and Immiscible Blends

    NASA Astrophysics Data System (ADS)

    Ling, Gerald H.; Shaw, Montgomery T.

    2008-07-01

    Polyethylene microgels were created by swollen-state grinding and ultrasonic fragmentation of bulk crosslinked polyethylene (XLPE) suspended in squalane, and by the extraction of crosslinked-polyethylene micro-domains from an immiscible blend of polyethylene (PE) and polystyrene (PS). Crosslinking of the polyethylene micro-domains in the blend was achieved by exposure to an electron beam. Suspensions of both microgels in squalane exhibit thermal gelation upon cooling where both G' and G″ increase by up to five-orders in magnitude when probed using small-angle oscillatory shear. We propose that this phenomenon is attributed to weak short-range interactions among the particles whereby surface terminal chains on the microgels can co-crystallize forming inter-particle bonds. However, these interactions are mild enough that the systems may be reverted to its original state by applying higher shear stresses at elevated temperatures.

  5. Postharvest storage quality of grapefruit placed in polyethylene bags with or without micro-perforation

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Washed ‘Marsh’ white grapefruit were placed in polyethylene (PE) bags (1 mil) with or without micro-perforation holes (representing 0.002% of the bag surface) and evaluated for juice quality, firmness, and the development of decay and disorders during storage for 30, 60, or 90 days at 50oF. Each tre...

  6. Functionalization enhancement on interfacial shear strength between graphene and polyethylene

    NASA Astrophysics Data System (ADS)

    Jin, Yikuang; Duan, Fangli; Mu, Xiaojing

    2016-11-01

    Pull-out processes were simulated to investigate the interfacial mechanical properties between the functionalized graphene sheet (FGS) and polyethylene (PE) matrix by using molecular dynamics simulation with ReaxFF reactive force field. The interfacial structure of polymer and the interfacial interaction in the equilibrium FGS/PE systems were also analyzed to reveal the enhancement mechanism of interfacial shear strength. We observed the insertion of functional groups into polymer layer in the equilibrium FGS/PE systems. During the pull-out process, some interfacial chains were attached on the FGS and pulled out from the polymer matrix. The behavior of these pulled out chains was further analyzed to clarify the different traction action of functional groups applied on them. The results show that the traction effect of functional groups on the pulled-out chains is agreement with their enhancement influence on the interfacial shear strength of the FGS/PE systems. They both are basically dominated by the size of functional groups, suggesting the enhancement mechanism of mechanical interlocking. However, interfacial binding strength also exhibits an obvious influence on the interfacial shear properties of the hybrid system. Our simulation show that geometric constrains at the interface is the principal contributor to the enhancement of interfacial shear strength in the FGS/PE systems, which could be further strengthened by the wrinkled morphology of graphene in experiments.

  7. No, Really: P.E. Online

    ERIC Educational Resources Information Center

    Stover, Del

    2005-01-01

    Because some students need to drop some extracurricular activities in order to enroll in a PE class, public schools have developed PE courses that can be fitted into students' tight schedules. These programs are popular because of convenience. Not only can workouts be scheduled as desired, but students can sweat it out almost anywhere: the local…

  8. Elementary Students' Construct of PE Teacher Credibility

    ERIC Educational Resources Information Center

    Ramos, Nilo O.; McCullick, Bryan A.

    2015-01-01

    The purpose of this study was to investigate elementary students' perceptions of PE teacher credibility. Eight high- and low-skilled students from grades 3 and 5 were selected from a school employing a PE teacher holding a National Board Certification. Data were collected in the school setting utilizing observations, field notes, an open-ended…

  9. Improvement of aluminum/polyethylene adhesion through corona discharge

    NASA Astrophysics Data System (ADS)

    Popelka, Anton; Krupa, Igor; Novák, Igor; Al-Maadeed, Mariam Ali S. A.; Ouederni, Mabrouk

    2017-01-01

    Polyethylene (PE) is often used in several industrial applications including the building, packaging and transport industries. Aluminum (Al) is widely used in different applications in the automotive, railway, aeronautic, and naval industries because of its excellent mechanical and chemical properties. Laminates prepared from Al and PE lead to an enhancement in physical and mechanical properties. These materials play a main role in the packaging and building sectors, such as in TetraPak containers and aluminum composite panels. The main problem observed is associated with the adhesion between polymers and metals. This research focused on investigating the enhancement in the adhesion of the PE/Al laminate using the corona discharge. The corona treatment of the surfaces led to a significant increase in the adhesion of the PE/Al laminate as a result of improved surface properties confirmed by peel test measurements. Moreover, the positive effect of the corona treatment in combination with a primer on the improvement of adhesion characteristics was observed too. Different analytical techniques were employed to characterize the effect of the corona treatment on the improvement in adhesion of PE/Al. A significant increase in wettability was confirmed by the measurement of contact angles. Changes in the surface morphology of the PE and Al surface, after the corona treatments at different operating conditions, were observed using atomic force microscopy (AFM) and scanning electron microscopy (SEM). In addition, x-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR) were used to analyze changes in chemical composition after the corona discharge effect on PE and Al surfaces.

  10. Structure and antibacterial properties of polyethylene/organo-vermiculite composites

    NASA Astrophysics Data System (ADS)

    Hundáková, Marianna; Tokarský, Jonáš; Valášková, Marta; Slobodian, Petr; Pazdziora, Erich; Kimmer, Dušan

    2015-10-01

    Vermiculite (VER) was modified by cation exchange with hexadecyltrimethylammonium (HDTMA+) bromide in three concentrations and used as organo-VER clay mineral nanofillers (denoted as HDTMA+1-VER, HDTMA+2-VER, and HDTMA+3-VER) in polyethylene (PE). PE/organo-VER composites were prepared via a melt compounding technique and pressed into thin plates. The organo-VER nanofillers and composite plates were characterized by X-ray diffraction analysis which in combination with molecular modeling confirmed the intercalation of HDTMA+ molecules. It was found that alkyl tails of HDTMA+ molecules create a non-polar, water-free area which may help the PE chains to enter the VER interlayer space. The nanocomposite structure was confirmed for PE/HDTMA+3-VER. PE/organo-VER composites were also studied by scanning electron microscopy and light microscopy and by creep testing. Antibacterial activity of powder organo-VER nanofillers was tested on Gram-positive (G+) (Staphylococcus aureus, Enterococcus faecalis) and Gram-negative (G-) (Escherichia coli) bacterial strains. The most sensitive G+ bacteria responded by stopping their bacterial growth after 24 h with a minimum inhibitory concentration (MIC) 0.014% (w/v) at all samples. Growth of G- bacteria was inhibited after 24 h with higher MIC value 0.041-10% (w/v) in relation to the content of HDTMA+ in samples. The surfaces of PE/organo-VER composites are very active against G+ bacterial strain E. faecalis. The number of bacterial colonies forming units (cfu) on surfaces of samples was reduced by approximately several orders. The number of bacterial colonies after 48 h was 0 cfu on the surface of PE/HDTMA+3-VER nanocomposite.

  11. Preparation of a new micro-porous poly(methyl methacrylate)-grafted polyethylene separator for high performance Li secondary battery

    NASA Astrophysics Data System (ADS)

    Gwon, Sung-Jin; Choi, Jae-Hak; Sohn, Joon-Yong; Ihm, Young-Eon; Nho, Young-Chang

    2009-10-01

    In this study, micro-porous poly(methyl methacrylate)-grafted polyethylene separators (PE-g-PMMA) were prepared by a radiation-induced graft polymerization of methyl methacrylate onto a conventional PE separator followed by a phase inversion. After the phase inversion, the micro-pores were generated in the grafted PMMA layer. The prepared micro-porous PE-g-PMMA separators showed an improved electrolyte uptake and ionic conductivity due to their improved affinity with a liquid electrolyte and the presence of pores in the grafted PMMA layer. The PE-g-PMMA separators exhibited a lower thermal shrinkage compared to the original PE separator. The PE-g-PMMA separators showed a better oxidation stability up to 5.0 V when compared to the original PE separator (4.5 V).

  12. Kinetics and microscopic processes of long term fracture in polyethylene piping materials. Final report, February 1, 1991-February 1, 1992

    SciTech Connect

    Brown, N.; Lu, X.

    1992-07-21

    The report contains 9 completed works as follows: The Dependence of Slow Crack Growth in a Polyethylene Copolymer on Testing Temperature and Morphology; A Test of Slow Crack Growth Failure of PE under Constant Load; Effect of Annealing on Slow Crack Growth in an Ethylene-Hexene Copolymer; The Fundamental Material Parameters that Govern Slow Crack Growth in Linear Polyethylene; Slow Crack Growth in Blends of HDPE and UHMWPE; The Mechqnism of Fatigue Failure in a Polyethylene Copolymer; PENT Quality Control Test for PE Gas Pipes and Resins; International Round Robin Study of A Fatigue Test Approach to the Ranking of Polyethylene Pipe Material; Proposed ASTM Specification for ASTM F17.40 Test Methods Committee.

  13. Graphite/Ultra-High Modulus Polyethylene Hybrid Fiber Composites with Epoxy and Polyethylene Matrices for Cosmic Radiation Shielding

    NASA Technical Reports Server (NTRS)

    2003-01-01

    One of the most significant technical challenges in long-duration space missions is that of protecting the crew from harmful radiation. Protection against such radiation on a manned Mars mission will be of vital importance both during transit and while on the surface of the planet. The development of multifunctional materials that serve as integral structural members of the space vehicle and provide the necessary radiation shielding for the crew would be both mission enabling and cost effective. Additionally, combining shielding and structure could reduce total vehicle mass. Hybrid laminated composite materials having both ultramodulus polyethylene (PE) and graphite fibers in epoxy and PE matrices could meet such mission requirements. PE fibers have excellent physical properties, including the highest specific strength of any known fiber. Moreover, the high hydrogen (H) content of polyethylene makes the material an excellent shielding material for cosmic radiation. When such materials are incorporated into an epoxy or PE matrix a very effective shielding material is expected. Boron (B) may be added to the matrix resin or used as a coating to further increase the shielding effectiveness due to B s ability to slow thermal neutrons. These materials may also serve as micrometeorites shields due to PE s high impact energy absorption properties. It should be noted that such materials can be fabricated by existing equipment and methods. It is the objective of this work therefore to: (a) perform preliminary analysis of the radiation transport within these materials; (b) fabricate panels for mechanical property testing before and after radiation exposure. Preliminary determination on the effectiveness of the combinations of material components on both shielding and structural efficiency will be made.

  14. Influence of polyethylene glycol (PEG) chain length on the thermal behavior of spin-coated thin films of biodegradable poly(3-hydroxybutyrate-co-3-hydroxyhexanoate)/PEG blends

    NASA Astrophysics Data System (ADS)

    Chen, Yujing; Park, Yeonju; Noda, Isao; Jung, Young Mee

    2016-11-01

    The influence of the polyethylene glycol (PEG, Mn = 400, 1500, and 3400) chain length on the miscibility and thermal properties of spin-coated films of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (PHBHx, HHx = 6.9 mol %)/PEG blends was elucidated by using differential scanning calorimetry (DSC) and temperature-dependent infrared (IR) spectroscopy. To extract more detailed information about the spectral variations induced by the temperature, 2D correlation spectroscopy was applied to the temperature-dependent IR spectra of PHBHx/PEG blends. It was found that PEG 400 was completely miscible with PHBHx while PEG 1500 and 3400 were only partially miscible, reflecting that PHBHx/PEG miscibility decreased with the increasing molecular weight of PEG. The amorphous band of carbonyl group of 70/30 PHBHx/PEG 400 blend is resolved into two bands at 1744 and 1754 cm-1 in the asynchronous spectrum, which is not observed in the corresponding asynchronous 2D correlation spectra of PHBHx and its blend with PEG 1500 and 3400. This observation suggests that we captured the possible existence of two different types of amorphous state in 70/30 PHBHx/PEG 400 blend and the band at 1744 cm-1 is related to the amorphous mixture of PHBHx and PEG 400. Furthermore, 2D correlation analysis and the normalized peak height trends demonstrate that PEG 400 disrupts the crystalline structure of PHBHx, indicating low molecular weight PEG 400 has a clear effect on the thermal properties of PHBHx as well as depressing its melting temperature.

  15. Characteristics of Protons Exiting from a Polyethylene Converter Irradiated by Neutrons with Energies between 1 keV and 10 MeV

    PubMed Central

    Nikezic, D.; Shahmohammadi Beni, Mehrdad; Krstic, D.; Yu, K. N.

    2016-01-01

    Monte Carlo method has been used to determine the efficiency for proton production and to study the energy and angular distributions of the generated protons. The ENDF library of cross sections is used to simulate the interactions between the neutrons and the atoms in a polyethylene (PE) layer, while the ranges of protons with different energies in PE are determined using the Stopping and Range of Ions in Matter (SRIM) computer code. The efficiency of proton production increases with the PE layer thickness. However the proton escaping from a certain polyethylene volume is highly dependent on the neutron energy and target thickness, except for a very thin PE layer. The energy and angular distributions of protons are also estimated in the present paper, showing that, for the range of energy and thickness considered, the proton flux escaping is dependent on the PE layer thickness, with the presence of an optimal thickness for a fixed primary neutron energy. PMID:27362656

  16. Method for casting polyethylene pipe

    NASA Technical Reports Server (NTRS)

    Elam, R. M., Jr.

    1973-01-01

    Short lengths of 7-cm ID polyethylene pipe are cast in a mold which has a core made of room-temperature-vulcanizable (RTV) silicone. Core expands during casting and shrinks on cooling to allow for contraction of the polyethylene.

  17. Films

    NASA Astrophysics Data System (ADS)

    Li, Ming; Zhang, Yang; Shao, Yayun; Zeng, Min; Zhang, Zhang; Gao, Xingsen; Lu, Xubing; Liu, J.-M.; Ishiwara, Hiroshi

    2014-09-01

    In this paper, we investigated the microstructure and electrical properties of Bi2SiO5 (BSO) doped SrBi2Ta2O9 (SBT) films deposited by chemical solution deposition. X-ray diffraction observation indicated that the crystalline structures of all the BSO-doped SBT films are nearly the same as those of a pure SBT film. Through BSO doping, the 2Pr and 2Ec values of SBT films were changed from 15.3 μC/cm2 and 138 kV/cm of pure SBT to 1.45 μC/cm2 and 74 kV/cm of 10 wt.% BSO-doped SBT. The dielectric constant at 1 MHz for SBT varied from 199 of pure SBT to 96 of 10 wt.% BSO-doped SBT. The doped SBT films exhibited higher leakage current than that of non-doped SBT films. Nevertheless, all the doped SBT films still had small dielectric loss and low leakage current. Our present work will provide useful insights into the BSO doping effects to the SBT films, and it will be helpful for the material design in the future nonvolatile ferroelectric memories.

  18. Kinetics and microscopic processes of long-term fracture in polyethylene-piping materials. Annual report, February 1, 1989-February 1, 1990

    SciTech Connect

    Brown, N.; Lu, X.

    1990-05-10

    Contents: notchology--the effect of the notching method on the slow crack growth failure in tough polyethylene; the effect of molecular weight on the fatigue behavior of high density polyethylene; the transition from ductile to slow crack growth failure in a copolymer of polyethylene; the ductile-brittle transition in a polyethylene copolymer; a unification of ductile failure and slow crack growth in an ethylene-octene copolymer; the dependence of butyl branch density on slow crack growth in polyethylene-kinetics; slow crack growth under fatigue and constant stress for ethylene-hexene resins with different density of branches; correlation of the fatigue test and the constant load slow crack growth test; relationship between slow crack growth and morphological change in ethylene-hexene copolymers; morphological changes on annealing in hdpe and mdpe and their effect on slow crack growth; ranking of pe gas pipe resins in air and igepal; brittle fracture of pe at low temperature; butt fusion welding.

  19. Effective Blending of Ultrahigh Molecular Weight Polyethylene with High-Density Polyethylene via Solid-State Shear Pulverization (SSSP)

    NASA Astrophysics Data System (ADS)

    Diop, Mirian; Torkelson, John

    2014-03-01

    Compared with conventional polyolefins, ultrahigh molecular weight polyethylene (UHMWPE) possesses outstanding mechanical properties, including impact strength and crack resistance, that make it it highly desirable for applications ranging from body armor to implants. Unfortunately, UHMWPE has an ultrahigh melt viscosity that renders common melt processes ineffective for making products from UHMWPE. Attempts to overcome this problem by blending UHMWPE with polyethylene (PE) by conventional melt mixing have been unsuccessful because of the enormous viscosity mismatch between blend components and have led to large suspensions of UHMWPE particles within a PE matrix. Here, we show the utility of solid-state shear pulverization (SSSP) in achieving effectively and intimately mixed UHMWPE/PE blends. For blends with up to 50 wt% UHMWPE we observe only slight increases in viscosity (η) at high shear rates but major increases in η with increasing UHMWPE content at low shear rates. Using extensional rheology, we confirm the strain hardening behavior of SSSP blends. Additionally, shear rheology and differential scanning calorimetry data indicate that the degree of mixing between UHMWPE and HDPE domains can be increased dramatically with subsequent passes of SSSP and single screw extrusion. Finally, blends prepared via SSSP show dramatic increases in impact strength; e.g., for a 30/70 wt% UHMWPE/HDPE blend, impact strength increases by about 300 % (relative to the parent neat HDPE).

  20. Method for shaping polyethylene tubing

    NASA Technical Reports Server (NTRS)

    Kramer, R. C.

    1981-01-01

    Method forms polyethylene plastic tubing into configurations previously only possible with metal tubing. By using polyethylene in place of copper or stain less steel tubing inlow pressure systems, fabrication costs are significantly reduced. Polyethylene tubing can be used whenever low pressure tubing is needed in oil operations, aircraft and space applications, powerplants, and testing laboratories.

  1. Synthesis and characterization of azo acrylates grafted onto polyethylene terephthalate by gamma irradiation

    NASA Astrophysics Data System (ADS)

    Bucio, Emilio; Skewes, Phill; Burillo, Guillermina

    2005-07-01

    Polyethylene terephthalate (PET) films were grafted with acryloyl chloride by gamma irradiation, and the grafted films were reacted with Disperse Red 1 or 4-phenylazophenol. The films where characterized by atomic force microscopy, differential scanning calorimetry, FTIR-ATR, light polarized microscopy, elemental analysis and UV spectroscopy. The surface of the films was homogeneous, and the dye underwent trans to cis photoreaction, whereby the red films became colorless by the irradiation of UV light at room temperature.

  2. Plasma treated polyethylene grafted with adhesive molecules for enhanced adhesion and growth of fibroblasts.

    PubMed

    Rimpelová, Silvie; Kasálková, Nikola Slepičková; Slepička, Petr; Lemerová, Helena; Švorčík, Václav; Ruml, Tomáš

    2013-04-01

    The cell-material interface plays a crucial role in the interaction of cells with synthetic materials for biomedical use. The application of plasma for tailoring polymer surfaces is of abiding interest and holds a great promise in biomedicine. In this paper, we describe polyethylene (PE) surface tuning by Ar plasma irradiating and subsequent grafting of the chemically active PE surface with adhesive proteins or motives to support cell attachment. These simple modifications resulted in changed polymer surface hydrophilicity, roughness and morphology, which we thoroughly characterized. The effect of our modifications on adhesion and growth was tested in vitro using mouse embryonic fibroblasts (NIH 3T3 cell line). We demonstrate that the plasma treatment of PE had a positive effect on the adhesion, spreading, homogeneity of distribution and moderately on proliferation activity of NIH 3T3 cells. This effect was even more pronounced on PE coated with biomolecules.

  3. Atmospheric-Pressure Non-thermal Plasma-JET effects on PS and PE surfaces

    NASA Astrophysics Data System (ADS)

    Arrieta, J.; Asenjo, J.; Vargas, I.; Solis, Y.

    2015-03-01

    The Atmospheric-Pressure Non-Thermal Plasma (APNTP) has become a topic of a great interest for a wide spectrum of applications in different industry branches, including the surface of treatment processes. In this work we evaluate the effect of an argon APNTP exposure to determine changes suffered by a polystyrene (PS) and polyethylene (PE) polymer surface through RAMAN spectroscopy and SEM. It was determined that the hydrophilic change in energetic terms, i.e. surface activation in the PS and PE polymers is addition of oxygen by surface activation when the samples with jet plasma are exposed with the inert argon gas. It was possible to characterize the hydrophilic shift based on the change in intensity of the spectra.

  4. Precision Polyolefin Structure: Modeling Polyethylene Containing Methyl and Ethyl Branches

    NASA Astrophysics Data System (ADS)

    Rojas, Giovanni; Wagener, Kenneth B.

    Sequenced copolymers of ethylene and diverse species have been created using acyclic diene metathesis (ADMET) polymerization, a step growth, condensation- type polymerization driven to high conversion by the removal of ethylene. ADMET permits control over branch content and branch length, which can be predetermined during the monomer synthesis, allowing sequence control in the resultant unsaturated polymer. Monomers are symmetrical α,ωdienes with a pendant functionality. Diverse functional groups are compatible with ADMET polymerization when Schrock’s or first-generation Grubb’s catalysts are used. Saturation with hydrogen after ADMET polymerization affords a polyethylene (PE) backbone bearing specific functionalities in precise places. Varying both the pendant functional group and the spacing between functionalities alters the physical and chemical properties of the polymer. Incorporation of alkyl chains into the PE backbone via ADMET leads to the study of perfect structures modeling the copolymerization of ethylene with α-olefins such as 1-propene, 1-butene, 1-hexene, and 1-octene.

  5. Development of flexible antimicrobial films using essential oils as active agents.

    PubMed

    López, P; Sánchez, C; Batlle, R; Nerín, C

    2007-10-17

    The antimicrobial activity in the vapor-phase of laboratory-made flexible films of polypropylene (PP) and polyethylene/ethylene vinyl alcohol copolymer (PE/EVOH) incorporating essential oil of cinnamon ( Cinnamomum zeylanicum), oregano ( Origanum vulgare), clove ( Syzygium aromaticum), or cinnamon fortified with cinnamaldehyde was evaluated against a wide range of microorganisms: the Gram-negative bacteria Escherichia coli, Yersinia enterocolitica, Pseudomonas aeruginosa, and Salmonella choleraesuis; the Gram-positive bacteria Listeria monocytogenes, Staphylococcus aureus, Bacillus cereus, and Enterococcus faecalis; the molds Penicillium islandicum, Penicillium roqueforti, Penicillium nalgiovense, Eurotium repens, and A spergillus flavus and the yeasts Candida albicans, Debaryomyces hansenii, and Zigosaccharomyces rouxii. Films with a nominal concentration of 4% (w/w) of fortified cinnamon or oregano essential oil completely inhibited the growth of the fungi; higher concentrations were required to inhibit the Gram-positive bacteria (8 and 10%, respectively), and higher concentrations still were necessary to inhibit the Gram-negative bacteria. PP films were more effective than PE/EVOH films. The atmospheres generated by the antimicrobial films inside Petri dishes were quantitatively analyzed using headspace-single drop microextraction (HS-SDME) in combination with gas chromatography-mass spectrometry (GC-MS). The analyses showed that the oregano-fortified PP films released higher levels of carvacrol and thymol, and the cinnamon-fortified PP films released higher levels of cinnamaldehyde, during the first 3-6 h of incubation, than the corresponding PE/EVOH films. Shelf-life tests were also performed, demonstrating that the antifungal activities of the films persisted for more than two months after their manufacture. In addition, migration tests (overall and specific) were performed, using both aqueous and fatty simulants, to ensure that the films meet EU regulations

  6. Unraveling the luminescence signatures of chemical defects in polyethylene

    SciTech Connect

    Chen, Lihua; Tran, Huan Doan; Wang, Chenchen; Ramprasad, Rampi

    2015-09-28

    Chemical defects in polyethylene (PE) can deleteriously downgrade its electrical properties and performance. Although these defects usually leave spectroscopic signatures in terms of characteristic luminescence peaks, it is nontrivial to make unambiguous assignments of the peaks to specific defect types. In this work, we go beyond traditional density functional theory calculations to determine intra-defect state transition and charge recombination process derived emission and absorption energies in PE. By calculating the total energy differences of the neutral defect at excited and ground states, the emission energies from intra-defect state transition are obtained, reasonably explaining the photoluminescence peaks in PE. In order to study the luminescence emitted in charge recombination processes, we characterize PE defect levels in terms of thermodynamic and optical charge transition levels that involve total energy calculations of neutral and charged defects. Calculations are performed at several levels of theory including those involving (semi)local and hybrid electron exchange-correlation functionals, and many-body perturbation theory. With these critical elements, the emission energies are computed and further used to clarify and confirm the origins of the observed electroluminescence and thermoluminescence peaks.

  7. Effect of polymer viscosities on the fiber structure and membrane properties of polypropylene/polyethylene bicomponent hollow fibers

    NASA Astrophysics Data System (ADS)

    Sugiura, Satoshi; Takarada, Wataru; Kikutani, Takeshi

    2015-05-01

    Polypropylene (PP) / Polyethylene (PE) bicomponent microporous hollow fiber membranes were prepared through the bicomponent melt spinning and drawing processes. Fibers of hollow shape were firstly prepared through the melt spinning process by introducing the air into the core part of the fiber cross-section. Annealing and drawing processes were applied to thus prepared fibers to furnish the membrane properties to the fibers. In this study, high and low molecular weight PP, HMwPP and LMwPP, were used. Viscosity of HMwPP was higher than that of PE, while viscosity of LMwPP was lower than that of PE. In the case of LMwPP/PE fibers, birefringence of PE component increased with take-up velocity and birefringence of LMwPP component was lower than that of PE component at all attainable take-up velocities. In HMwPP/PE fibers, birefringence of both components increased with take-up velocity at low take-up velocities. Birefringence of HMwPP component increased continuously with further increase of take-up velocity, however that of PE component decreased significantly at the take-up velocity higher than 1 km/min. In this region, birefringence of HMwPP component in HMwPP/PE bicomponent hollow fibers was much higher than that of LMwPP component in LMwPP/PE hollow fibers. Hollow fiber membrane which was prepared by annealing and drawing of HMwPP/PE hollow fibers showed 10 times higher air transmission rate than that of LMwPP/PE fibers. In addition, air transmission rate increased with an increase in the HMwPP composition. These results indicate that the structure of PP component in the as-spun fiber undertake a crucial role on membrane properties in PP/PE bicomponent hollow fiber membrane.

  8. Thermal Decomposition of Copper Ore Concentrate and Polyethylene Composites

    NASA Astrophysics Data System (ADS)

    Szyszka, Danuta; Wieckowska, Jadwiga

    2016-10-01

    Thermal analyses (TGA and DTA) of the composite, comprised of 10% polyethylene (PE) scrap and 90% copper ore concentrate, enabled determination of the temperature range and decomposition degree of the organic matters in argon atmosphere. Products of pyrolysis were qualitatively and quantitatively determined. The results were compared to those obtained for products of pyrolysis of the composite in air. Products of pyrolysis were identified by means of the gas chromatography (GC) method alone or supported with results of mass spectrometry analyses (GC-MS).

  9. Does cyclic stress and accelerated ageing influence the wear behavior of highly crosslinked polyethylene?

    PubMed

    Affatato, Saverio; De Mattia, Jonathan Salvatore; Bracco, Pierangiola; Pavoni, Eleonora; Taddei, Paola

    2016-06-01

    First-generation (irradiated and remelted or annealed) and second-generation (irradiated and vitamin E blended or doped) highly crosslinked polyethylenes were introduced in the last decade to solve the problems of wear and osteolysis. In this study, the influence of the Vitamin-E addition on crosslinked polyethylene (XLPE_VE) was evaluated by comparing the in vitro wear behavior of crosslinked polyethylene (XLPE) versus Vitamin-E blended polyethylene XLPE and conventional ultra-high molecular weight polyethylene (STD_PE) acetabular cups, after accelerated ageing according to ASTM F2003-02 (70.0±0.1°C, pure oxygen at 5bar for 14 days). The test was performed using a hip joint simulator run for two millions cycles, under bovine calf serum as lubricant. Mass loss was found to decrease along the series XLPE_VE>STD_PE>XLPE, although no statistically significant differences were found between the mass losses of the three sets of cups. Micro-Raman spectroscopy was used to investigate at a molecular level the morphology changes induced by wear. The spectroscopic analyses showed that the accelerated ageing determined different wear mechanisms and molecular rearrangements during testing with regards to the changes in both the chain orientation and the distribution of the all-trans sequences within the orthorhombic, amorphous and third phases. The results of the present study showed that the addition of vitamin E was not effective to improve the gravimetric wear of PE after accelerated ageing. However, from a molecular point of view, the XLPE_VE acetabular cups tested after accelerated ageing appeared definitely less damaged than the STD_PE ones and comparable to XLPE samples.

  10. Transcriptomics and lipidomics of the environmental strain Rhodococcus ruber point out consumption pathways and potential metabolic bottlenecks for polyethylene degradation.

    PubMed

    Gravouil, Kevin; Ferru-Clement, Romain; Colas, Steven; Helye, Reynald; Kadri, Linette; Bourdeau, Ludivine; Moumen, Bouziane; Mercier, Anne; Ferreira, Thierry

    2017-03-27

    Polyethylene (PE), one of the most prominent synthetic polymer used worldwide, is very poorly biodegradable in the natural environment. Consequently, PE represents by itself more than half of all plastic wastes. PE biodegradation is achieved through the combination of abiotic and biotic processes. Several microorganisms have been shown to grow on the surface of PE materials, among which are the species of the Rhodococcus genus, suggesting a potent ability of these microorganisms to use, at least partly, PE as a potent carbon source. However, most of them, if not all, fail to induce a clear-cut degradation of PE samples, showing that bottlenecks to reach optimal biodegradation clearly exist. To identify the pathways involved in PE consumption, we used in the present study a combination of RNA-sequencing and lipidomic strategies. We show that short-term exposure to various forms of PE, displaying different molecular weight distributions and oxidation levels, lead to an increase in the expression of 158 genes in a Rhodococcus representative, R. ruber. Interestingly, one of the most up-regulated pathways is related to alkane degradation and β-oxidation of fatty acids. This approach also allowed us to identify metabolic limiting steps, which could be fruitfully targeted for optimized PE consumption by R. ruber.

  11. Improved adhesion, growth and maturation of vascular smooth muscle cells on polyethylene grafted with bioactive molecules and carbon particles.

    PubMed

    Parizek, Martin; Kasalkova, Nikola; Bacakova, Lucie; Slepicka, Petr; Lisa, Vera; Blazkova, Martina; Svorcik, Vaclav

    2009-11-20

    High-density polyethylene (PE) foils were modified by an Ar(+) plasma discharge and subsequent grafting with biomolecules, namely glycine (Gly), polyethylene glycol (PEG), bovine serum albumin (BSA), colloidal carbon particles (C) or BSA and C (BSA + C). As revealed by atomic force microscopy (AFM), goniometry and Rutherford Backscattering Spectroscopy (RBS), the surface chemical structure and surface morphology of PE changed dramatically after plasma treatment. The contact angle decreased for the samples treated by plasma, mainly in relation to the formation of oxygen structures during plasma irradiation. A further decrease in the contact angle was obvious after glycine and PEG grafting. The increase in oxygen concentration after glycine and PEG grafting proved that the two molecules were chemically linked to the plasma-activated surface. Plasma treatment led to ablation of the PE surface layer, thus the surface morphology was changed and the surface roughness was increased. The materials were then seeded with vascular smooth muscle cells (VSMC) derived from rat aorta and incubated in a DMEM medium with fetal bovine serum. Generally, the cells adhered and grew better on modified rather than on unmodified PE samples. Immunofluorescence showed that focal adhesion plaques containing talin, vinculin and paxillin were most apparent in cells on PE grafted with PEG or BSA + C, and the fibres containing alpha-actin, beta-actin or SM1 and SM2 myosins were thicker, more numerous and more brightly stained in the cells on all modified PE samples than on pristine PE. An enzyme-linked immunosorbent assay (ELISA) revealed increased concentrations of focal adhesion proteins talin and vinculin and also a cytoskeletal protein beta-actin in cells on PE modified with BSA + C. A contractile protein alpha-actin was increased in cells on PE grafted with PEG or Gly. These results showed that PE activated with plasma and subsequently grafted with bioactive molecules and colloidal C

  12. Improved Adhesion, Growth and Maturation of Vascular Smooth Muscle Cells on Polyethylene Grafted with Bioactive Molecules and Carbon Particles

    PubMed Central

    Parizek, Martin; Kasalkova, Nikola; Bacakova, Lucie; Slepicka, Petr; Lisa, Vera; Blazkova, Martina; Svorcik, Vaclav

    2009-01-01

    High-density polyethylene (PE) foils were modified by an Ar+ plasma discharge and subsequent grafting with biomolecules, namely glycine (Gly), polyethylene glycol (PEG), bovine serum albumin (BSA), colloidal carbon particles (C) or BSA and C (BSA + C). As revealed by atomic force microscopy (AFM), goniometry and Rutherford Backscattering Spectroscopy (RBS), the surface chemical structure and surface morphology of PE changed dramatically after plasma treatment. The contact angle decreased for the samples treated by plasma, mainly in relation to the formation of oxygen structures during plasma irradiation. A further decrease in the contact angle was obvious after glycine and PEG grafting. The increase in oxygen concentration after glycine and PEG grafting proved that the two molecules were chemically linked to the plasma-activated surface. Plasma treatment led to ablation of the PE surface layer, thus the surface morphology was changed and the surface roughness was increased. The materials were then seeded with vascular smooth muscle cells (VSMC) derived from rat aorta and incubated in a DMEM medium with fetal bovine serum. Generally, the cells adhered and grew better on modified rather than on unmodified PE samples. Immunofluorescence showed that focal adhesion plaques containing talin, vinculin and paxillin were most apparent in cells on PE grafted with PEG or BSA + C, and the fibres containing α-actin, β-actin or SM1 and SM2 myosins were thicker, more numerous and more brightly stained in the cells on all modified PE samples than on pristine PE. An enzyme-linked immunosorbent assay (ELISA) revealed increased concentrations of focal adhesion proteins talin and vinculin and also a cytoskeletal protein β-actin in cells on PE modified with BSA + C. A contractile protein α-actin was increased in cells on PE grafted with PEG or Gly. These results showed that PE activated with plasma and subsequently grafted with bioactive molecules and colloidal C particles

  13. Polyethylene glycol as a solid polymer electrolyte

    SciTech Connect

    Cha, D.K.; Park, S.M.

    1997-12-01

    Polymer electrolytes were prepared from polyethylene glycol (PEG)-lithium perchlorate complexes and characterized at a stainless steel electrode using a variety of electrochemical techniques. The charge transfer process was affected by the oxide film on the stainless steel electrode surface in the early stages of redox processes. The polymer electrolytes showed a transference number of 0.2 for Li{sup +}. The conductivity of the PEG-10000 electrolyte has been determined to be 4.7 {times} 10{sup {minus}5} S/cm. This rather high value is attributed to the anionic end groups increasing the polarity of the matrix.

  14. Influence of structure on radiation shielding effectiveness of graphite fiber reinforced polyethylene composite

    NASA Astrophysics Data System (ADS)

    Emmanuel, A.; Raghavan, J.

    2015-10-01

    While LEO and GEO are used for most satellite missions, Highly Elliptical Orbits (HEOs) are also used for satellite missions covering Polar Regions of Earth. Satellites in HEO are exposed to a relatively harsher radiation environment than LEO and GEO. The mass of traditionally used aluminum radiation shield, required to attenuate the radiation to a level below a certain threshold that is safe for the satellite bus and payload, scales with the level of radiation. It has been shown (Emmanuel et al., 2014) that materials with low atomic number (Z) such as polyethylene (PE) can result in a lighter shield than aluminum (Al) in HEO. However, PE has to be reinforced with relatively high Z fibers such as graphite (G) to improve its mechanical properties. The effect of introduction of G and the resulting composite structure (that meets the requirements on mechanical properties, manufacturing and service) on the radiation shielding effectiveness of PE was studied through simulation using a layered PE-G composite. The Total Ionization Dose (TID), deposited in a silicon detector behind the composite shield, has been found to be function of layer volume fraction, layer thickness and stacking sequence of the PE and G layers. One composite configuration has resulted in a TID lower than that for PE, demonstrating the possibility of tailoring the mechanical properties of PE-based composite radiation shield with minimal negative impact on its radiation shielding effectiveness.

  15. Boehmite particle coating modified microporous polyethylene membrane: A promising separator for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Yang, Chongwen; Tong, Hua; Luo, Chuanpeng; Yuan, Shuanglong; Chen, Guorong; Yang, Yunxia

    2017-04-01

    To exploit high-quality separators for lithium ion batteries, current research activities are mainly focused on the modification of microporous polyolefin membranes by coating them with inorganic particles to achieve comprehensive improvements in their thermal stability, electrochemical compatibility, and overcharge protection. Here, we report a separator made by coating boehmite (AlOOH) particles on microporous polyethylene (PE) membranes. Compared to the commercially applied coating materials, e.g., aluminum oxide (Al2O3), AlOOH allows for a substantial reduction in the coating thickness, while ensuring excellent thermal stability of the modified PE membrane. Our study shows that this is due to the formation of an interlocking interface structure that interconnects the PE membrane and AlOOH coating layer as soon as PE melts at about 140 °C, preventing the modified PE membrane from shrinking at subsequently elevated temperatures. The modified PE membrane exhibits suitable electrolyte wettability to facilitate ion transport through it. Thus, the lithium ion batteries employing it as a separator could attain substantially improved electrochemical performance. Furthermore, the AlOOH-coated PE separator was also found to provide an excellent overcharge protection.

  16. Polyethylene-water partitioning coefficients for parent- and alkylated-polycyclic aromatic hydrocarbons and polychlorinated biphenyls.

    PubMed

    Choi, Yongju; Cho, Yeo-Myoung; Luthy, Richard G

    2013-07-02

    We report polyethylene (PE)-water partitioning coefficients (K(PE)) for 17 parent-polycyclic aromatic hydrocarbons (PAHs), 22 alkylated-PAHs, 3 perdeuterated parent-PAHs, and 100 polychlorinated biphenyl (PCB) congeners or coeluting congener groups. The K(PE) values for compounds in the same homologue group are within 0.2 log units for alkylated-PAHs but span up to an order of magnitude for PCBs, due to the greater contribution of the position of the substituents (i.e., chlorines for PCBs and alkyl groups for alkylated-PAHs) to the molecular structure. The K(PE) values in deionized water for parent- and alkylated-PAHs show a good correlation with a regression model employing the number of aromatic carbons (C(AR)) and aliphatic carbons (C(AL)) in each compound: log K(PE) = -0.241 + 0.313 C(AR) + 0.461 C(AL). The regression model is useful for the assessment of freely dissolved aqueous concentrations of alkylated-PAHs, which comprise a significant fraction of the total in petroleum-derived PAHs and in some pyrogenic PAH mixtures. For PCBs, experimentally determined octanol-water partitioning coefficients are the best predictor of the K(PE) values among the molecular parameters studied. The effect of salinity up to 20 or 30 parts per thousand is found to be relatively insignificant on K(PE) values for PAHs or PCBs, respectively.

  17. Degradation of degradable starch-polyethylene plastics in a compost environment

    SciTech Connect

    Johnson, K.E.; Pometto, A.L. III; Nikolov, Z.L. )

    1993-04-01

    Degradable plastics have differing degradation rates. Three types of degradation of polyethylene in the starch-polyethylene polymers can occur: chemical degradation, photodegradation, and biological degradation. This study examines all three types of degradation in 11 commercially produced degradable starch-polyethylene bags. Different rates for chemical and photo-degradation were found within a 20 day or an 8-week period. Results indicated that both the 70[degree]C oven and HT-HH film treatments were appropriate methods to evaluate oxidative degradation. In a compost environment, oxygen tension on the surface of the film appears to be the rate-limiting component for both chemical and biological degradation. Levels of starch in all bags was similar, so the prooxidant additive was critical in promoting the oxidative degradation of polyethylene. The Fe-Mn additive displayed the best catalytic activity. This study overall confirms degradation of starch-polyethylene plastics in a natural environment. 17 refs., 6 figs., 2 tabs.

  18. Controlling Miscibility in Polyethylene-Polynorbornene Block Copolymers via Side-Group Chemistry

    NASA Astrophysics Data System (ADS)

    Mulhearn, William; Register, Richard

    Block copolymers containing a crystallizable block, such as polyethylene (PE), and an amorphous block with high glass transition temperature (Tg) are an interesting class of materials since the rigid glassy block can improve the mechanical response of the article under strain by reinforcing the crystal fold surface. However, to prepare an easily processable PE-containing block copolymer it is necessary to avoid microphase separation in the melt by selection of amorphous blocks with weak repulsive interactions against PE (low Flory interaction parameter χ or interaction energy density X) . Most such low- χ polymers are chemically similar to PE, such as copolymers of ethylene and a small amount of an α-olefin, and therefore exhibit similarly low glass transition temperatures. This work investigates a series of low- and high-Tg polymers based on substituted norbornene monomers, polymerized via ring-opening metathesis polymerization (ROMP). Hydrogenated polynorbornene derivatives possess a wide range of glass transition temperatures, and miscibility with PE can be readily tuned by the choice of substituents on the monomers (e.g. aromatic vs. aliphatic groups). Two species investigated, hydrogenated poly(cyclohexyl norbornene) and hydrogenated poly(norbornyl norbornene), have high Tg and also remain miscible with polyethylene to high molecular weight. Furthermore, we develop a set of mixing rules to qualitatively predict the solubility behavior of substituted ROMP polynorbornenes as a function of their side-groups.

  19. Unravelling the potential of nitric acid as a surface modifier for improving the hemocompatibility of metallocene polyethylene for blood contacting devices

    PubMed Central

    Vellayappan, Muthu Vignesh; Muhamad, Ida Idayu

    2016-01-01

    Design of blood compatible surfaces is obligatory to minimize platelet surface interactions and improve the thromboresistance of foreign surfaces when they are utilized as biomaterials particularly for blood contacting devices. Pure metallocene polyethylene (mPE) and nitric acid (HNO3) treated mPE antithrombogenicity and hydrophilicity were investigated. The contact angle of the mPE treated with HNO3 decreased. Surface of mPE and HNO3 treated mPE investigated with FTIR revealed no major changes in its functional groups. 3D Hirox digital microscopy, SEM and AFM images show increased porosity and surface roughness. Blood coagulation assays prothrombin time (PT) and activated partial thromboplastin time (APTT) were delayed significantly (P < 0.05) for HNO3 treated mPE. Hemolysis assay and platelet adhesion of the treated surface resulted in the lysis of red blood cells and platelet adherence, respectively indicating improved hemocompatibility of HNO3 treated mPE. To determine that HNO3 does not deteriorate elastic modulus of mPE, the elastic modulus of mPE and HNO3 treated mPE was compared and the result shows no significant difference. Hence, the overall observation suggests that the novel HNO3 treated mPE may hold great promises to be exploited for blood contacting devices like grafts, catheters, and etc. PMID:26819837

  20. Wear resistance of artificial hip joints with poly(2-methacryloyloxyethyl phosphorylcholine) grafted polyethylene: comparisons with the effect of polyethylene cross-linking and ceramic femoral heads.

    PubMed

    Moro, Toru; Kawaguchi, Hiroshi; Ishihara, Kazuhiko; Kyomoto, Masayuki; Karita, Tatsuro; Ito, Hideya; Nakamura, Kozo; Takatori, Yoshio

    2009-06-01

    Aseptic loosening of artificial hip joints induced by wear particles from the polyethylene (PE) liner remains the ruinous problem limiting their longevity. We reported here that grafting with a polymer, poly(2-methacryloyloxyethyl phosphorylcholine (MPC)) (PMPC), on the PE liner surface dramatically decreased the wear production under a hip joint simulator condition. We examined that the effect of properties of both PE by cross-linking and femoral head by changing the materials on wearing properties of PE. The PMPC grafting on the liners increased hydrophilicity and decreased friction torque, regardless of the cross-linking of the PE liner or the difference in the femoral head materials. During the hip joint simulator experiments (5 x 10(6) cycles of loading), cross-linking caused a decrease of wear amount and a reduction of the particle size, while the femoral head materials did not affect it. The PMPC grafting abrogated the wear production, confirmed by almost no wear of the liner surface, independently of the liner cross-linking or the femoral head material. We concluded that the PMPC grafting on the PE liner surpasses the liner cross-linking or the change of femoral head materials for extending longevity of artificial hip joints.

  1. Effect of Sliding Speed and Contract Stress on Tribological Properties of Ultra-High-Molecular-Weight Polyethylene.

    DTIC Science & Technology

    1982-11-01

    hemispherically tipped AIST 44OC high-temperature (HT) stainless-steel riders sliding against ultra-high- molecular-weight polyethylene ( UHMwPE ) disks. The surface...others who used different specimen configurations. The results indicate that sliding speed, sliding distance, contact stress, and specimen geometry can all markedly influence the tribological properties of UHMWPE . (MM)

  2. Fabrication of Tunable Submicro- or Nano-structured Polyethylene Materials form Immiscible Blends with Cellulose Acetate Butyrate

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Low density polyethylene (LDPE) was prepared into micro- or submicro-spheres or nanofibers via melt blending or extrusion of cellulose acetate butyrate (CAB)/LDPE immiscible blends and subsequent removal of the CAB matrix. The sizes of the PE spheres or fibers can be successfully controlled by varyi...

  3. Space charge behaviour in maleic anhydride grafted polyethylene/ethylene - vinyl - acetate copolymer laminates

    NASA Astrophysics Data System (ADS)

    Lee, Seung Hyung; Park, Jung Ki; Han, Jae Hong; Suh, Kwang S.

    1997-01-01

    Charge distributions in maleic anhydride (MAH) grafted polyethylene (g-PE)/ethylene - vinyl - acetate (EVA) copolymer laminates have been measured with materials of different composition. All laminates showed interfacial charge, the polarity and the magnitude of which are explained by interfacial polarization. It was found that the interfacial charge increased with the increase of MAH content in the g-PE, whereas it decreased with the increase of vinyl - acetate content in the EVA. This feature was attributed to the differences in electrical conductivity of the materials. Details of the experimental results are described.

  4. Mixed Micelles made of Poly(ethylene glycol)-Phosphatidylethanolamine Conjugate and D-α-tocopheryl Polyethylene Glycol 1000 Succinate as Pharmaceutical Nanocarriers for Camptothecin

    PubMed Central

    Mu, L.; Elbayoumi, T.A.; Torchilin, V.P.

    2006-01-01

    Micelles from the mixture of poly(ethylene glycol)-phosphatidyl ethanolamine conjugate (PEG-PE) and D-α-tocopheryl polyetheyene glycol 1000 succinate (TPGS) were prepared loaded with the poorly soluble anticancer drug camptothecin (CPT). The solubilization of CPT by the mixed micelles was more efficient than with earlier described micelles made of PEG-PE alone. CPT-loaded mixed micelles were stable upon storage and dilution and firmly retained the incorporated drug. The cytotoxicity of the CPT-loaded mixed micelles against various cancer cells in vitro was remarkably higher than that of the free drug. PEG-PE/TPGS mixed micelles may serve as pharmaceutical nanocarriers with improved solubilization capacity for poorly soluble drugs. PMID:16242875

  5. Investigations of the intermolecular forces between RDX and polyethylene by force-distance spectroscopy and molecular dynamics simulations.

    PubMed

    Taylor, D E; Strawhecker, K E; Shanholtz, E R; Sorescu, D C; Sausa, R C

    2014-07-10

    The development of novel nanoenergetic materials with enhanced bulk properties requires an understanding of the intermolecular interactions occurring between molecular components. We investigate the surface interactions between 1,3,5-trinitro-1,3,5-triazacyclohexane (RDX) and polyethylene (PE) crystals on the basis of combined use of molecular dynamics (MD) simulations and force-distance spectroscopy, in conjunction with Lifshitz macroscopic theory of van der Waals forces between continuous materials. The binding energy in the RDX-PE system depends both on the degree of PE crystallinity and on the RDX crystal face. Our MD simulations yield binding energies of approximately 132 and 120 mJ/m(2) for 100% amorphous and 100% crystalline PE on RDX (210), respectively. The average value is about 36% greater than our experimental value of 81 ± 15 mJ/m(2) for PE (∼48% amorphous) on RDX (210). By comparison, Liftshitz theory predicts a value of about 79 mJ/m(2) for PE interacting with RDX. Our MD simulations also predict larger binding energies for both amorphous and crystalline PE on RDX (210) compared to the RDX (001) surface. Analysis of the interaction potential indicates that about 60% of the binding energy in the PE-RDX system is due to attractive interactions between HPE-ORDX and CPE-NRDX pairs of atoms. Further, amorphous PE shows a much longer interaction distance than crystalline PE with the (210) and (001) RDX surfaces due to the possibility of larger polymer elongations in the case of amorphous PE as strain is applied. Also, we report estimates of the binding energies of energetic materials RDX and octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX) with PE, propylene, polystyrene, and several fluorine-containing polymers using Lifshitz theory and compare these with reported MD calculations.

  6. Polarimetric studies of polyethylene terephtalate flexible substrates

    NASA Astrophysics Data System (ADS)

    Stchakovsky, M.; Garcia-Caurel, E.; Warenghem, M.

    2008-12-01

    Polymer sheets are currently used worldwide in a wide range of applications. The manufacturing process of these sheets involves extruding machines that stretch the material in both lateral and longitudinal directions with respect to the machine direction, thus inducing birefringence. In most cases, the film obtained is optically biaxial. Polarimetric spectroscopy (Ellipsometry and Mueller Matrix) combined with conoscopic observation are the methods of choice to study these properties. In this work we report an analysis of commercially available polyethylene terephtalate (PET) films used as substrate for food packaging as well as for embedded electronic devices such as solar cells or flexible displays. Initial observation of these films through polarizing microscope in conoscopic mode reveals first the trace of optical axis plane with respect to the film surface and second, whether the optical axis is acute or not. This preliminary study allows optimal sample positioning for further polarimetric studies. The measurements and modelling are done in both reflection and transmission mode on several spectroscopic polarimetric setups from UV to NIR. The models give as a main result, the dielectric tensor of the film as well as its orientation with respect to the laboratory reference frame.

  7. Morphological characteristics of waste polyethylene/polypropylene plastics during pyrolysis and representative morphological signal characterizing pyrolysis stages.

    PubMed

    Wang, H; Chen, D; Yuan, G; Ma, X; Dai, X

    2013-02-01

    In this work, the morphological characteristics of waste polyethylene (PE)/polypropylene (PP) plastics during their pyrolysis process were investigated, and based on their basic image changing patterns representative morphological signals describing the pyrolysis stages were obtained. PE and PP granules and films were used as typical plastics for testing, and influence of impurities was also investigated. During pyrolysis experiments, photographs of the testing samples were taken sequentially with a high-speed infrared camera, and the quantitative parameters that describe the morphological characteristics of these photographs were explored using the "Image Pro Plus (v6.3)" digital image processing software. The experimental results showed that plastics pyrolysis involved four stages: melting, two stages of decomposition which are characterized with bubble formation caused by volatile evaporating, and ash deposition; and each stage was characterized with its own phase changing behaviors and morphological features. Two stages of decomposition are the key step of pyrolysis since they took up half or more of the reaction time; melting step consumed another half of reaction time in experiments when raw materials were heated up from ambient temperatures; and coke-like deposition appeared as a result of decomposition completion. Two morphological signals defined from digital image processing, namely, pixel area of the interested reaction region and bubble ratio (BR) caused by volatile evaporating were found to change regularly with pyrolysis stages. In particular, for all experimental scenarios with plastics films and granules, the BR curves always exhibited a slowly drop as melting started and then a sharp increase followed by a deep decrease corresponding to the first stage of intense decomposition, afterwards a second increase - drop section corresponding to the second stage of decomposition appeared. As ash deposition happened, the BR dropped to zero or very low

  8. Polyethylene Glycol Propionaldehydes

    NASA Technical Reports Server (NTRS)

    Harris, Joe M.; Sedaghat-Herati, Mohammad R.; Karr, Laurel J.

    1992-01-01

    New class of compounds derived from polyethylene glycol (PEG's) namely, PEG-propionaldehydes, offers two important advantages over other classes of PEG aldehyde derivatives: compounds exhibit selective chemical reactivity toward amino groups and are stable in aqueous environment. PEG's and derivatives used to couple variety of other molecules, such as, to tether protein molecules to surfaces. Biotechnical and biomedical applications include partitioning of two phases in aqueous media; immobilization of such proteins as enzymes, antibodies, and antigens; modification of drugs; and preparation of protein-rejecting surfaces. In addition, surfaces coated with PEG's and derivatives used to control wetting and electroosmosis. Another potential application, coupling to aminated surfaces.

  9. Preparation of nanocomposite γ-Al2O3/polyethylene separator crosslinked by electron beam irradiation for lithium secondary battery

    NASA Astrophysics Data System (ADS)

    Nho, Young-Chang; Sohn, Joon-Yong; Shin, Junhwa; Park, Jong-Seok; Lim, Yoon-Mook; Kang, Phil-Hyun

    2017-03-01

    Although micro-porous membranes made of polyethylene (PE) offer excellent mechanical strength and chemical stability, they exhibit large thermal shrinkage at high temperature, which causes a short circuit between positive and negative electrodes in cases of unusual heat generation. We tried to develop a new technology to reduce the thermal shrinkage of PE separators by introducing γ-Al2O3 particles treated with coupling agent on PE separators. Nanocomposite γ-Al2O3/PE separators were prepared by the dip coating of polyethylene(PE) separators in γ-Al2O3/poly(vinylidenefluoride-hexafluoropropylene) (PVDF-HFP)/crosslinker (1,3,5-trially-1,3,5-triazine-2,4,6(1 H,3 H,5 H)-trione (TTT) solution with humidity control followed by electron beam irradiation. γ-Al2O3/PVDF-HFP/TTT (95/5/2)-coated PE separator showed the highest electrolyte uptake (157%) and ionic conductivity (1.3 mS/cm). On the basis of the thermal shrinkage test, the nanocomposite γ-Al2O3/PE separators containing TTT irradiated by electron beam exhibited a higher thermal resistance. Moreover, a linear sweep voltammetry test showed that the irradiated nanocomposite γ-Al2O3/PE separators have electrochemical stabilities of up to 5.0 V. In a battery performance test, the coin cell assembled with γ-Al2O3/PVDF-HFP/TTT-coated PE separator showed excellent discharge cycle performance.

  10. School PE through Internet Discussion Forums

    ERIC Educational Resources Information Center

    Lauritsalo, Kirsti; Sääkslahti, Arja; Rasku-Puttonen, Helena

    2015-01-01

    Background: Physical education is a subject that generates strong feelings and emotions, as can be seen in written accounts of PE experiences. It is also important to listen to students' voices in the research context. Nowadays, students can be listened to in a new way--through the Internet. Various discussion forums on the Internet make it…

  11. Mechanical and thermal properties of short-coirfiber-reinforced natural rubber/polyethylene composites

    NASA Astrophysics Data System (ADS)

    Xu, Zh. H.; Kong, Zh. N.

    2014-07-01

    Natural rubber (NR) and polyethylene (PE) composites were compounded with chemically treated coir fibers by using a heated two-roll mill. Two chemical treatments of the fibers — by silane and sodium hydroxide — were carried out to improve the interfacial adhesion between them and the polyethylene matrix. The mechanical properties of the composites obtained were evaluated and compared with those made from a neat polymer and untreated fibers. The mechanical properties of the composites, such as the tensile strength, Young's modulus, and the elongation at break, were examined, and their shrinkage and flame retardant characteristics were measured. From these experiments, the effect of plasma treatment on the mechanical-physical behavior of coconut-fiberreinforced NR/PE composites was identified. In addition, their thermal characteristics were evaluated, and the results showed a slight decrease in them with increasing content of coir fibers.

  12. Adsorption and association of a symmetric PEO-PPO-PEO triblock copolymer on polypropylene, polyethylene, and cellulose surfaces.

    PubMed

    Li, Yan; Liu, Hongyi; Song, Junlong; Rojas, Orlando J; Hinestroza, Juan P

    2011-07-01

    The association of a symmetric polyoxyethylene-polyoxypropylene-polyoxyethylene (PEO(19)-PPO(29)-PEO(19)) triblock copolymer adsorbed from aqueous solutions onto polypropylene (PP), polyethylene (PE), and cellulose surfaces was probed using Atomic Force Microscopy (AFM). Significant morphological differences between the polyolefin substrates (PP and PE) and the cellulose surfaces were observed after immersion of the films in the PEO(19)-PPO(29)-PEO(19) solutions. When the samples were scanned, while immersed in solutions of the triblock copolymer, it was revealed that the structures adsorbed on the polyolefin surfaces were smoothed by the adsorbed PEO(19)-PPO(29)-PEO(19). In contrast, those structures on the hydrophilic cellulose surfaces were sharpened. These observations were related to the roughness of the substrate and the energy of interaction between the surfaces and the PEO and PPO polymer segments. The interaction energy between each of the blocks and the surface was calculated using molecular dynamics simulations. It is speculated that the associative structures amply reported in aqueous solution at concentrations above the critical micelle concentration, CMC, are not necessarily preserved upon adsorption; instead, it appears that molecular arrangements of the anchor-buoy type and hemimicelles prevail. The reported data suggests that the roughness of the surface, as well as its degree of hydrophobicity, have a large influence on the nature of the resulting adsorbed layer. The reported observations are valuable in explaining the behavior of finishing additives and lubricants commonly used in textile and fiber processing, as well as the effect of the morphology of the boundary layers on friction and wear, especially in the case of symmetric triblock copolymers, which are commonly used as antifriction, antiwear additives.

  13. EFFECTS OF TRITIUM EXPOSURE ON UHMW-PE, PTFE, AND VESPEL

    SciTech Connect

    Clark, E; Kirk Shanahan, K

    2006-05-31

    Samples of three polymers, Ultra-High Molecular Weight Polyethylene (UHMW-PE), polytetrafluoroethylene (PTFE, also known as Teflon{reg_sign}), and Vespel{reg_sign} polyimide were exposed to 1 atmosphere of tritium gas at ambient temperature for varying times up to 2.3 years in closed containers. Sample mass and size measurements (to calculate density), spectra-colorimetry, dynamic mechanical analysis (DMA), and Fourier-transform infrared spectroscopy (FT-IR) were employed to characterize the effects of tritium exposure on these samples. Changes of the tritium exposure gas itself were characterized at the end of exposure by measuring total pressure and by mass spectroscopic analysis of the gas composition. None of the polymers exhibited significant changes of density. The color of initially white UHMW-PE and PTFE dramatically darkened to the eye and the color also significantly changed as measured by colorimetry. The bulk of UHMW-PE darkened just like the external surfaces, however the fracture surface of PTFE appeared white compared to the PTFE external surfaces. The white interior could have been formed while the sample was breaking or could reflect the extra tritium dose at the surface directly from the gas. The dynamic mechanical response of UHMW-PE was typical of radiation effects on polymers- an initial stiffening (increased storage modulus) and reduction of viscous behavior after three months exposure, followed by lowering of the storage modulus after one year exposure and longer. The storage modulus of PTFE increased through about nine months tritium exposure, then the samples became too weak to handle or test using DMA. Characterization of Vespel{reg_sign} using DMA was problematic--sample-to-sample variations were significant and no systematic change with tritium exposure could be discerned. Isotopic exchange and incorporation of tritium into UHMW-PE (exchanging for protium) and into PTFE (exchanging for fluorine) was observed by FT-IR using an attenuated

  14. Modification of polyethylene by radiation-induced graft polymerization of acrylic acid

    NASA Astrophysics Data System (ADS)

    Sidorova, L. P.; Aliev, A. D.; Zlobin, V. B.; Aliev, R. E.; Chalykh, A. E.; Kabanov, V. Ya.

    The kinetics investigation of the radiation-induced graft polymerization of acrylic acid onto low density polyethylene by direct method in aqueous solution in the presence of Mohr's salt, was performed. The technique of the contrasting of polyacrylic acid (PAA) graft layer was worked out by Ag +-ions. The structural and morphological peculiarities of grafted copolymers of PE with PAA were determined by the method of electron probe, and X-ray microanalysis by means of the electron microscopy.

  15. The radiation improvement of polyethylene prostheses. A preliminary study.

    PubMed

    Grobbelaar, C J; du Plessis, T A; Marais, F

    1978-08-01

    The radiation crosslinking of high-density polyethylene prostheses was investigated over a wide range of doses in the presence and absence of gaseous crosslinking agents. It was found that in the bulk polymer the crosslinking pattern is completely different from the homogeneous crosslinking that occurs in polymer films. The presence of crosslinking agents causes highly crosslinked polymer to be formed on the surface while the bulk of the polymer is largely unaffected--which is explained in terms of diffusion phenomena. This surface crosslinking has a profound effect on the mechanical properties of the prostheses and restricts cold flow and deformation of the polymer without sacrificing the excellent abrasion-resistance properties of the polyethylene when subjected to high pressures. Based on this research a number of high-density polyethylene knee prostheses have been radiation-crosslinked and the results in vitro appear to be very promising.

  16. What Is the PE Password? Incorporating Vocabulary in Your Elementary PE Program

    ERIC Educational Resources Information Center

    Robelee, Margaret E.

    2016-01-01

    This article describes a novel program for third through fifth grade called "What is the PE Password?" that teaches vocabulary words and concepts without sacrificing activity time in order to support Common Core learning.

  17. Shock wave propagation in semi-crystalline polyethylene: An atomic-scale investigation

    NASA Astrophysics Data System (ADS)

    Elder, Robert M.; O'Connor, Thomas C.; Yeh, In-Chul; Chantawansri, Tanya L.; Sirk, Timothy W.; Robbins, Mark O.; Andzelm, Jan W.

    Highly oriented polyethylene (PE) fibers are used in protection applications, therefore elucidation of their response under high strain-rate impact events is vital. Although PE fibers can have high crystallinity (>95%), they also contain defects such as amorphous domains. Using molecular dynamics simulations, we investigate shock propagation through crystalline, amorphous, and semi-crystalline PE. We generate compressive shock waves of varying strength, quantify their dynamics, and characterize their effect on material properties at the atomic scale. In the semi-crystalline PE model, the differing density and molecular order of amorphous PE and crystalline PE result in differing shock impedances, which causes reflection and refraction of shock waves at interfaces between the phases. We quantify the properties (e.g. pressure, velocity) of the reflected and refracted waves, which differ from those of the incident wave, and compare with results from impedance matching. We also examine the reflection, absorption, and transmission of energy at the crystalline-amorphous interface. Depending on shock strength, amorphous defects can dissipate shock energy, which attenuates the shock and leads to effects such as localized heating.

  18. Triple shape memory effects of cross-linked polyethylene/polypropylene blends with cocontinuous architecture.

    PubMed

    Zhao, Jun; Chen, Min; Wang, Xiaoyan; Zhao, Xiaodong; Wang, Zhenwen; Dang, Zhi-Min; Ma, Lan; Hu, Guo-Hua; Chen, Fenghua

    2013-06-26

    In this paper, the triple shape memory effects (SMEs) observed in chemically cross-linked polyethylene (PE)/polypropylene (PP) blends with cocontinuous architecture are systematically investigated. The cocontinuous window of typical immiscible PE/PP blends is the volume fraction of PE (v(PE)) of ca. 30-70 vol %. This architecture can be stabilized by chemical cross-linking. Different initiators, 2,5-dimethyl-2,5-di(tert-butylperoxy)-hexane (DHBP), dicumylperoxide (DCP) coupled with divinylbenzene (DVB) (DCP-DVB), and their mixture (DHBP/DCP-DVB), are used for the cross-linking. According to the differential scanning calorimetry (DSC) measurements and gel fraction calculations, DHBP produces the best cross-linking and DCP-DVB the worst, and the mixture, DHBP/DCP-DVB, is in between. The chemical cross-linking causes lower melting temperature (Tm) and smaller melting enthalpy (ΔHm). The prepared triple shape memory polymers (SMPs) by cocontinuous immiscible PE/PP blends with v(PE) of 50 vol % show pronounced triple SMEs in the dynamic mechanical thermal analysis (DMTA) and visual observation. This new strategy of chemically cross-linked immiscible blends with cocontinuous architecture can be used to design and prepare new SMPs with triple SMEs.

  19. Investigation of the influence factors of polyethylene molecule encapsulated into carbon nanotubes by molecular dynamics simulation

    NASA Astrophysics Data System (ADS)

    Li, Qun; He, Guofang; Zhao, Rengao; Li, Yanfei

    2011-09-01

    In this work, the influence factors, namely chirality, temperature, radius and surface chemical modification, of the interaction energy for polyethylene (PE) molecule encapsulated into single-walled carbon nanotubes (SWNTs) had been investigated by molecular mechanics (MM) and molecular dynamics (MD) simulation. The results showed that all these factors would influence the interaction energy between PE and SWNTs. The interaction energy between PE molecule and the armchair SWNTs is largest among eight kinds of chiral SWNTs. The interaction energy decreases with the increase of temperature or the SWNT radius. The methyl, phenyl, hydroxyl, carboxyl, -F, and amino groups, have been introduced onto the surface of the SWNTs by the simulation software and the influence of SWNT chemical modification has also been investigated. The interaction energy between PE and chemically modified SWNTs is larger than that between PE and pristine SWNTs, and increases with increasing the concentration of the modified groups monotonously. In addition, the group electronegativity and van der Waals force will affect the interaction energy between PE and chemically modified SWNTs greatly, which can be attributed to the electronic structures of the chemically modified groups. This study can provide some useful suggestions for the composite material design and drug transport.

  20. Initial Stages of Pyrolysis of Polyethylene

    NASA Astrophysics Data System (ADS)

    Popov, Konstantin V.

    Combustion and flammability of plastics are important topics of practical interest directly related to fire safety and recycling of polymeric materials; pyrolysis of the solid is the initial step of its combustion. One of the main ways to study such complicated processes is through detailed mechanistic modeling, in which the process is represented by a set of many elementary reactions. Mechanistic modeling of combustion of plastics is considerably hindered by the lack of necessary kinetic data. In virtually all existing models of polymer pyrolysis the majority of kinetic data used are derived from the corresponding gas phase values of smaller species. The use of gas phase rate constants is, generally, not justified without an experimental justification. In the first part of the work the influence of condensed phase on the rate of scission of a carbon-carbon bond (the reaction that initiates pyrolysis and combustion) in polyethylene (PE) was studied using the method of Reactive Molecular Dynamics (RMD). A method based on a two-step kinetic mechanism was developed to decouple the cage effect from the kinetics of the reaction under study. It was observed that under the conditions of condensed phase the rate constant of C-C bond scission in PE decreased by an order of magnitude compared to that obtained in vacuum. It was also shown that under the conditions of polymer melt the rate constant does not depend on the length of the polymer chain. In the second part of the work the kinetics of liquid phase and gas phase products of PE pyrolysis were studied experimentally using Gas Chromatography and Nuclear Magnetic Resonance. Based on the assumption of applicability of gas phase kinetic data for C-C scission reaction and beta-scission reaction under the conditions of polymer melt, rate constants of hydrogen transfer, radical addition to double bonds, and radical recombination were determined via kinetic modeling of the experimental results. The obtained values of the rate

  1. An Evaluation of Polycyclic Aromatic Hydrocarbon Uptake into Polyethylene Samplers

    NASA Astrophysics Data System (ADS)

    Martynowych, D. J.; McDonough, C.; Lohmann, R.

    2013-12-01

    Polyethylene passive samplers (PEs) are simple reliable tools that have been widely used in the detection of hydrophobic organic compounds. Thick (>200μm or greater) PEs have important applications to specific sampling scenarios including biological assays, deployment on ships and aircraft (towing) and long term sampling, however little is known about their uptake kinetics. This study aimed to develop an accurate understanding of the uptake kinetics of these thick PEs. PE passive samplers of equal surface area, but differing thicknesses were co-deployed in the surface water and air of lower Narragansett Bay in 2013 to characterize differences in their uptake of polycyclic aromatic hydrocarbons (PAHs). PE samplers of approximately 50, 800, and 1600μm thicknesses were analyzed for 38 parent and alkylated PAHs, with replicate sampler reproducibility mostly within 25%. A number of smaller PAHs (typically those with a molecular weight less than 180) analyzed over a 4 week deployment equilibrated, while the larger molecules remained in the linear or curve linear uptake stages. Results from a second, 24 week deployment of 800μm and 1600μm samplers in surface waters suggest that all 38 compounds studied remained in the linear uptake stage. The PE-weight normalized concentration ratio of 1600μm to 800μm sampler fell below 1 for all analytes, implying equilibrium had not been established.

  2. Molecular Dynamics Study of Polyethylene under Extreme Confinement

    NASA Astrophysics Data System (ADS)

    Kritikos, G.; Sgouros, A.; Vogiatzis, G. G.; Theodorou, D. N.

    2016-08-01

    We present results concerning the dynamics and the structure of adsorbed layers of molten polyethylene (PE) between two graphite surfaces. The molecular weight of the monodisperse PE chains reaches the entanglement regime. We study three cases of interwall distances, equal to two, three and four times the unperturbed radius of gyration (Rg ) of PE chains. The confined system is equilibrated by use of efficient Monte Carlo (MC) algorithms. Conducting molecular dynamics (MD) simulations, we reveal the distribution of relaxation times as a function of distance from the graphite walls at the temperature of 450 K. From the atomic-level stresses we calculate a realistic estimate of the adhesion tension, which is not affected significantly by the width of the pore. Although the distance between the two walls is comparable to the width of the adsorbed layer, we do not record the formation of ‘glassy bridges’ under the studied conditions. The diffusion of polymer chains in the middle layer is not inhibited by the existence of the two adsorbed layers. Extreme confinement conditions imposed by the long range wall potentials bring about an increase in both the adsorption and desorption rates of chains. The presented results seem to cohere with a reduction in the calorimetric (heat capacity step) glass transition temperature (Tg ).

  3. Carvacrol affects interfacial, structural and transfer properties of chitosan coatings applied onto polyethylene.

    PubMed

    Kurek, Mia; Brachais, Claire-Hélène; Sčetar, Mario; Voilley, Andrée; Galić, Kata; Couvercelle, Jean-Pierre; Debeaufort, Frédéric

    2013-08-14

    Different chitosan coating solutions were tested with the aim of investigating their adhesion and wettability onto polyethylene film to improve packaging performance and provide antimicrobial properties. Surface wetting kinetics was monitored by contact angle measurements. Addition of ethanol and carvacrol improved wettability and adhesion of the thin chitosan layer. Structure, water vapour, O2, CO2 and air permeabilities of self supported chitosan films and coated polyethylene were determined. The formation of a thin chitosan layer on polyethylene improved gas barrier properties decreasing the Permeability Coefficient for oxygen and carbon dioxide ( [Formula: see text] , [Formula: see text] ) from 100 to 10,000 times. Presence of carvacrol in the chitosan coating layer increased [Formula: see text] , [Formula: see text] and Pair by a factor of ten. Moreover, it influenced film microstructure. However chitosan was shown to be good gas barrier film in the dry state.

  4. Bio-compatibility of ion beam-modified and RGD-grafted polyethylene

    NASA Astrophysics Data System (ADS)

    Ročková-Hlaváčková, K.; Švorčík, V.; Bačáková, L.; Dvořánková, B.; Heitz, J.; Hnatowicz, V.

    2004-09-01

    Polyethylene (PE) was implanted with 15 keV Ar + and Kr + ions to the fluences from 3 × 10 12-1 × 10 15 cm -2 and subsequently grafted with amino acid sequence Arg-Gly-Asp (RGD), i.e. a minimum adhesion motif recognized by integrin receptors on cells. The structural changes of PE were studied using goniometric technique, UV-VIS, LIF spectroscopy and by measuring specimen electrical resistance. The adhesion and proliferation of mouse embryonic fibroblasts 3T3 on the modified PE were studied under in vitro conditions. Addition of RGD sequence onto double bonds created by the ion irradiation on polymeric chain was observed. The adhesion and proliferation of the 3T3 cells is increased by ion implantation and additionally also by RGD grafting.

  5. Correlation between free-volume parameters and physical properties of polyethylene-nitrile rubber blend

    NASA Astrophysics Data System (ADS)

    Gomaa, E.; Mostafa, N.; Mohsen, M.; Mohammed, M.

    2004-10-01

    Positron annihilation lifetime spectroscopy (PALS) was used to study the immiscibility of a polar nitrile rubber (NBR) that had been blended with pure and waste, low- and high-density polyethylene (PE). The effect of the weight percent of the rubber added to the PE was also investigated. It was found that a complicated variation (positive and negative) in both free-volume parameters (τ3 and I 3) from the values of the initial polymers forms an immiscible blend. These results are supported by a significant broadening in the free-volume hole size distributions. This has been interpreted in terms of interfacial spaces created between the boundaries of the two phases. Furthermore, a correlation was established between the free-volume parameters (τ3 and I 3) and the electrical and mechanical properties of the before mentioned polymer blends as a function of the weight percent of waste PE.

  6. The non-equilibrium phase diagrams of flow-induced crystallization and melting of polyethylene

    NASA Astrophysics Data System (ADS)

    Wang, Zhen; Ju, Jianzhu; Yang, Junsheng; Ma, Zhe; Liu, Dong; Cui, Kunpeng; Yang, Haoran; Chang, Jiarui; Huang, Ningdong; Li, Liangbin

    2016-09-01

    Combining extensional rheology with in-situ synchrotron ultrafast x-ray scattering, we studied flow-induced phase behaviors of polyethylene (PE) in a wide temperature range up to 240 °C. Non-equilibrium phase diagrams of crystallization and melting under flow conditions are constructed in stress-temperature space, composing of melt, non-crystalline δ, hexagonal and orthorhombic phases. The non-crystalline δ phase is demonstrated to be either a metastable transient pre-order for crystallization or a thermodynamically stable phase. Based on the non-equilibrium phase diagrams, nearly all observations in flow-induced crystallization (FIC) of PE can be well understood. The interplay of thermodynamic stabilities and kinetic competitions of the four phases creates rich kinetic pathways for FIC and diverse final structures. The non-equilibrium flow phase diagrams provide a detailed roadmap for precisely processing of PE with designed structures and properties.

  7. The non-equilibrium phase diagrams of flow-induced crystallization and melting of polyethylene

    PubMed Central

    Wang, Zhen; Ju, Jianzhu; Yang, Junsheng; Ma, Zhe; Liu, Dong; Cui, Kunpeng; Yang, Haoran; Chang, Jiarui; Huang, Ningdong; Li, Liangbin

    2016-01-01

    Combining extensional rheology with in-situ synchrotron ultrafast x-ray scattering, we studied flow-induced phase behaviors of polyethylene (PE) in a wide temperature range up to 240 °C. Non-equilibrium phase diagrams of crystallization and melting under flow conditions are constructed in stress-temperature space, composing of melt, non-crystalline δ, hexagonal and orthorhombic phases. The non-crystalline δ phase is demonstrated to be either a metastable transient pre-order for crystallization or a thermodynamically stable phase. Based on the non-equilibrium phase diagrams, nearly all observations in flow-induced crystallization (FIC) of PE can be well understood. The interplay of thermodynamic stabilities and kinetic competitions of the four phases creates rich kinetic pathways for FIC and diverse final structures. The non-equilibrium flow phase diagrams provide a detailed roadmap for precisely processing of PE with designed structures and properties. PMID:27609305

  8. Investigation of the formation of peroxide in. gamma. -irradiated polyethylene by the method of iodometric titration

    SciTech Connect

    Savost'yanov, V.S.; Kritskaya, D.A.; Ponomarev, A.N.

    1986-09-01

    The concentrations of hydroperoxides (HP) and dialkyl peroxides (DAP) in polyethylene (PE) powder, ..gamma.. irradiated in air at 295 K at a dose of 0.22-2.8 J/(kg x sec) up to doses of 16-300 kJ/kg, were determined by various methods of iodometric titration. Under the indicated conditions, the HP concentration reached 0.18 mole/kg, DPA 0.07 mole/kg, G /SUB HP/ was 8.3 1/100 eV; G /SUB GP/ ..integral..I /SUP -0.5/ . On the basis of the total absence of grafting of acrylamide onto ..gamma..-irradiated PE after reduction during titration of HP in it, it was concluded that grafted polymerization is initiated by the radicals of thermal decomposition of HP in PE.

  9. In vitro and in vivo imaging of ultra-high-molecular-weight polyethylene orbital implants.

    PubMed

    Olszycki, Marek; Kozakiewicz, Marcin; Elgalal, Marcin; Majos, Agata; Stefanczyk, Ludomir

    2015-01-01

    The aim of this study is to compare magnetic resonance imaging (MRI) with computed tomography (CT) for visualization of an orbital alloplastic prosthesis made of ultra-high-molecular-weight polyethylene (UHMW-PE) both in vitro and in vivo. A study of 15 test implants from UHMW-PE visualized in vitro in CT and MRI and an in vivo visualization in a patient who suffered from orbital injury and underwent reconstructive surgery is presented. The postsurgery MRI showed the UHMW-PE material clearly, with no significant artifacts. The surrounding tissues could be satisfactorily evaluated. The CT scans did not present the graft material. Both techniques were sufficient tools for in vitro evaluation of the shape and measurement of the prosthesis.

  10. BIM LAU-PE: Seedlings in Microgravity

    NASA Astrophysics Data System (ADS)

    Gass, S.; Pennese, R.; Chapuis, D.; Dainesi, P.; Nebuloni, S.; Garcia, M.; Oriol, A.

    2015-09-01

    The effect of gravity on plant roots is an intensive subject of research. Sounding rockets represent a costeffective platform to study this effect under microgravity conditions. As part of the upcoming MASER 13 sounding rocket campaign, two experiments on Arabidopsis thaliana seedlings have been devised: GRAMAT and SPARC. These experiments are aimed at studying (1) the genes that are specifically switched on or off during microgravity, and (2) the position of auxin-transporting proteins during microgravity. To perform these experiments, RUAG Space Switzerland site of Nyon, in collaboration with the Swedish Space Corporation (SSC) and the University of Freiburg, has developed the BIM LAU-PE (Biolology In Microgravity Late Access Unit Plant Experiment). In the following an overview of the BIM LAU-PE design is presented, highlighting specific module design features and verifications performed. A particular emphasis is placed on the parabolic flight experiments, including results of the micro-g injection system validation.

  11. Simple introduction of sulfonic acid group onto polyethylene by radiation-induced cografting of sodium styrenesulfonate with hydrophilic monomers. [electron beam

    SciTech Connect

    Tsuneda, Satoshi; Saito, Kyoichi; Furusaki, Shintaro . Dept. of Chemical Engineering); Sugo, Takanobu; Makuuchi, Keizo . Takasaki Radiation Chemistry Research Establishment)

    1993-07-01

    The sulfonic acid (SO[sub 3]H) group was readily introduced into a polyethylene (PE) membrane by radiation-induced cografting of sodium styrenesulfonate (SSS) with hydrophilic monomers such as acrylic acid (AAc) and hydroxyethyl methacrylate (HEMA). The density of SSS grafted onto the PE membrane was determined as a function of molar ratio of hydrophilic monomer to SSS in the monomer mixture. Immersion of the electron-beam-irradiated PE membrane into the mixture of SSS and HEMA for 5 h at 323 K provided to the SO[sub 3]H density of 2.5 mol/kg of the H-type product.

  12. Search for D{sup 0}{yields}pe{sup +} and D{sup 0}{yields}pe{sup -}

    SciTech Connect

    Rubin, P.; Lowrey, N.; Mehrabyan, S.; Selen, M.; Wiss, J.; Mitchell, R. E.; Shepherd, M. R.; Besson, D.; Pedlar, T. K.; Cronin-Hennessy, D.; Gao, K. Y.; Hietala, J.; Kubota, Y.; Klein, T.; Poling, R.; Scott, A. W.; Zweber, P.; Dobbs, S.; Metreveli, Z.; Seth, K. K.

    2009-05-01

    We search for simultaneous baryon and lepton number violating decays of the D{sup 0} meson. Specifically, we use 281 pb{sup -1} of data taken on the {psi}(3770) resonance with the CLEO-c detector at the CESR collider to look for decays D{sup 0}{yields}pe{sup +}, D{sup 0}{yields}pe{sup +}, D{sup 0}{yields}pe{sup -}, and D{sup 0}{yields}pe{sup -}. We find no significant signals and set the following branching fraction upper limits: D{sup 0}{yields}pe{sup +}(D{sup 0}{yields}pe{sup +})<1.1x10{sup -5} and D{sup 0}{yields}pe{sup -}(D{sup 0}{yields}pe{sup -})<1.0x10{sup -5}, both at the 90% confidence level.

  13. 21 CFR 172.260 - Oxidized polyethylene.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Oxidized polyethylene. 172.260 Section 172.260... § 172.260 Oxidized polyethylene. Oxidized polyethylene may be safely used as a component of food, subject to the following restrictions: (a) Oxidized polyethylene is the basic resin produced by the...

  14. 21 CFR 177.1615 - Polyethylene, fluorinated.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Polyethylene, fluorinated. 177.1615 Section 177... Contact Surfaces § 177.1615 Polyethylene, fluorinated. Fluorinated polyethylene, identified in paragraph... prescribed conditions: (a) Fluorinated polyethylene food-contact articles are produced by modifying...

  15. 21 CFR 177.1620 - Polyethylene, oxidized.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Polyethylene, oxidized. 177.1620 Section 177.1620... Contact Surfaces § 177.1620 Polyethylene, oxidized. Oxidized polyethylene identified in paragraph (a) of... following prescribed conditions: (a) Oxidized polyethylene is the basic resin produced by the mild...

  16. Final report on the safety assessment of polyethylene.

    PubMed

    2007-01-01

    Polyethylene is an ethylene polymer used for a variety of purposes in cosmetics as an abrasive, adhesive, binder or bulking agent, an emulsion stabilizer, a film former, an oral care agent, and as a nonaqueous viscosity-increasing agent. Polyethylene is also used in food packaging materials and medical products, including prosthetics. The molecular weight of Polyethylene as used in cosmetics varies over a wide range. The lowest reported molecular weight is 198 Daltons and the highest is 150,000. In any given polymer preparation, there can be a broad range of molecular weights. Cellular and tissue responses to Polyethylene, determined as part of implant biocompatibility testing, include fibrous connective tissue build-up around the implant material that varies as a function of the physical form of the implant material. Specific assays for osteoblast proliferation and collagen synthesis demonstrated a reduction as a function of exposure to Polyethylene particles that is inversely related to particle size. The effect of Polyurethane particles on monocyte-derived macrophages, however, had a stimulatory effect, prolonging the survival of these cells in culture. The LD50 for Polyethylene, with an average molecular weight of 450, in rats was > 2000 mg/kg. For Polyethylene with an average molecular weight of 655, the LD50 was > 5.0 g/kg. Toxicity testing in rats shows no adverse effects at Polyethylene (molecular weight not given) doses of 7.95 g/kg or at 1.25%, 2.50%, or 5.00% in feed for 90 days. Dermal irritation studies on rabbits in which 0.5 g of Polyethylene (average molecular weight of 450) was administered in 0.5 ml of water caused no irritation or corrosive effects; Polyethylene with an average molecular weight of 655 was a mild irritant. Polyethylene (average molecular weight of 450) did not cause dermal sensitization in guinea pigs tested with 50% Polyethylene (w/w) in arachis oil BP. Polyethylene, with a molecular weight of 450 and a molecular weight of 655

  17. Polyethylene recycling: Waste policy scenario analysis for the EU-27.

    PubMed

    Andreoni, Valeria; Saveyn, Hans G M; Eder, Peter

    2015-08-01

    This paper quantifies the main impacts that the adoption of the best recycling practices together with a reduction in the consumption of single-use plastic bags and the adoption of a kerbside collection system could have on the 27 Member States of the EU. The main consequences in terms of employment, waste management costs, emissions and energy use have been quantified for two scenarios of polyethylene (PE) waste production and recycling. That is to say, a "business as usual scenario", where the 2012 performances of PE waste production and recycling are extrapolated to 2020, is compared to a "best practice scenario", where the best available recycling practices are modelled together with the possible adoption of the amended Packaging and Packaging Waste Directive related to the consumption of single-use plastic bags and the implementation of a kerbside collection system. The main results show that socio-economic and environmental benefits can be generated across the EU by the implementation of the best practice scenario. In particular, estimations show a possible reduction of 4.4 million tonnes of non-recycled PE waste, together with a reduction of around €90 million in waste management costs in 2020 for the best practice scenario versus the business as usual scenario. An additional 35,622 jobs are also expected to be created. In environmental terms, the quantity of CO2 equivalent emissions could be reduced by around 1.46 million tonnes and the net energy requirements are expected to increase by 16.5 million GJ as a consequence of the reduction in the energy produced from waste. The main analysis provided in this paper, together with the data and the model presented, can be useful to identify the possible costs and benefits that the implementation of PE waste policies and Directives could generate for the EU.

  18. Interfacial interactions between polyethylene matrix and clay layers in polyethylene/clay nanocomposites

    NASA Astrophysics Data System (ADS)

    Abu-Zurayk, R.

    2015-10-01

    Polyethylene/clay nanocomposites were prepared as blown films using different formulae (clay contents (4 and 6 wt%) and compatibilizer/clay ratio (1/2, 1.0, 2.0)). Structure and mechanical behaviour were tested. It was found that blown film extrusion process decreased the tactoids size and consequently enhanced the exfoliation degree of the clay layers inside the polymer matrix, which is due to the elongational stress during extrusion. Addition of clay had some effects on mechanical behaviour. There was an increase of yield strength (max 32%). Yield strength is related to the interfacial interaction between the polymer and the clay layers in the nanocomposites, which would be enhanced by enhancing the compatibility between polymer and clay layers. Correlation analysis showed good correlation between compatibility and interfacial interaction parameters, and between parameters of interfacial interaction, structure and yield strength.

  19. Equipment evaluation for low density polyethylene encapsulated nitrate salt waste at the Rocky Flats Plant

    SciTech Connect

    Yamada, W.I.; Faucette, A.M.; Jantzen, R.C.; Logsdon, B.W.; Oldham, J.H.; Saiki, D.M.; Yudnich, R.J.

    1993-08-30

    Mixed wastes at the Rocky Flats Plant (RFP) are subject to regulation by the Resource Conservation and Recovery Act (RCRA). Polymer solidification is being developed as a final treatment technology for several of these mixed wastes, including nitrate salts. Encapsulation nitrate salts with low density polyethylene (LDPE) has been the preliminary focus of the RFP polymer solidification effort. Literature reviews, industry surveys, and lab-scale and pilot-scale tests have been conducted to evaluate several options for encapsulating nitrate salts with LDPE. Most of the effort has focused on identifying compatible drying and extrusion technologies. Other processing options, specifically meltration and non-heated compounding machines, were also investigated. The best approach appears to be pretreatment of the nitrate salt waste brine in either a vertical or horizontal thin film evaporator followed by compounding of the dried waste with LDPE in an intermeshing, co-rotating, twin-screw extruder. Additional pilot-scale tests planned for the fall of 1993 should further support this recommendation. Preliminary evaluation work indicates that meltration is not possible at atmospheric pressure with the LDPE (Chevron PE-1409) provided by RFP. However, meltration should be possible at atmospheric pressure using another LDPE formulation with altered physical and rheological properties: Lower molecular weight and lower viscosity (Epoline C-15). Contract modifications are now in process to allow a follow-on pilot scale demonstration. Questions regarding changed safety and physical properties of the resultant LDPE waste form due to use of the Epoline C-15 will be addressed. No additional work with non-heated mixer compounder machines is planned at this time.

  20. Effects of compatibilization on the essential work of fracture parameters of in situ microfiber reinforced poly(ethylene terephtahalate)/polyethylene blend

    SciTech Connect

    Li Zhongming; Yang Wei; Xie Banghu; Yang, S.Y.; Yang Mingbo; Feng Jianmin; Huang Rui

    2003-11-26

    A novel in situ microfiber reinforced blend (MRB) based on poly(ethylene terephthalate) (PET) and polyethylene (PE) was prepared by extrusion-hot stretching-quenching process, and was compatibilized with ethylene vinyl acetate copolymer (EVA) in the presence of the transesterification reaction catalyst, dibutyltin oxide (DBTO). The effects of compatibilization on the essential work of fracture parameters in PET/PE MRB were examined. It is found that the specific essential work of fracture (w{sub e}) and the specific non-essential work of fracture (w{sub p}) were significantly increased, when adding 1 and 2.5 phr of EVA to PET/PE MRB and it was further increased with the addition of 0.5 phr of DBTO as the catalyst of the transesterification reaction. The fracture surfaces study by scanning electron microscope (SEM) further proved that EVA is a successful compatibilizer for PET/PP blend. The morphology study of the blends shows that the well-defined fibers with the diameter of several microns were generated in situ during melt extrusion-hot stretch-quenching processing.

  1. The "physiologically effective" correlates: peDk/L and peDk.

    PubMed

    Hill, R M

    1999-03-01

    Introduced here are two predictive parameters, peDk/L and peDk. The prefix pe- (for physiologically effective) indicates that such values are estimates of lens transmissibility (Dk/L) and material permeability (Dk) and have been derived through a reverse application of the Residual Hypoxia model of Smith, relating corneal response (in hypoxic stress units) to lens transmissibility (Dk/L). Here, using independent databases, physiological responses to simple oxygen pathways (one layer, one material) but of unknown Dk value were entered into that model to estimate the Dk/L and (then by calculation) the Dk value of single vision rigid gas permeable (RGP) contact lenses. Also demonstrated was the application of this strategy for estimation of composite (integrated) Dk/L and Dk values of complex (multi-layer, multi-material) oxygen pathways, wherein one or more material Dk values and/or one or more local thickness are unknown.

  2. FeOx-TiO2 Film with Different Microstructures Leading to Femtosecond Transients with Different Properties: Biological Implications under Visible Light

    PubMed Central

    Rtimi, Sami; Pulgarin, Cesar; Nadtochenko, Victor A.; Gostev, Fedor E.; Shelaev, Ivan V.; Kiwi, John

    2016-01-01

    This study presents the first report addressing the effect of FeOx-TiO2 films microstructure on the transients detected by fast spectroscopy related to the long-range bacterial inactivation performance. The different fast kinetic femtosecond transient spectroscopy is reported for each FeOx+TiO2 microstructure. The lifetime of the short transient-species and the oxidative intermediate radicals generated under light were identified. Co-sputtered FeOx-TiO2 on polyethylene films presenting random distribution for both oxides were compared with sequentially sputtered FeOx/TiO2 films made up only by FeOx in the topmost layers. The ratio FeOx:TiO2 was optimized to attain the highest photo-conversion. By X-ray fluorescence, the Fe:Ti ration was found to be ~1.4 in the film bulk and by XPS-etching a ratio of 4:1 was found on the photocatalyst top-most layers. For co-sputtered FeOx-TiO2-PE films, the FeOx-TiO2 heterojunction led to electron injection from the FeOx to lower-lying TiO2 trapping states. The film optical properties, particle size, roughness, hydrophobic-hydrophilic shift and temporal evolution of the transient redox states were characterized in detail. Films with different microstructure led to different antibacterial activity. This suggests that the FeOx-TiO2-PE microstructure and not the position of the potential energy level of the semiconductors FeOx and TiO2 control the charge transfer under light irradiation. PMID:27443505

  3. FeOx-TiO2 Film with Different Microstructures Leading to Femtosecond Transients with Different Properties: Biological Implications under Visible Light

    NASA Astrophysics Data System (ADS)

    Rtimi, Sami; Pulgarin, Cesar; Nadtochenko, Victor A.; Gostev, Fedor E.; Shelaev, Ivan V.; Kiwi, John

    2016-07-01

    This study presents the first report addressing the effect of FeOx-TiO2 films microstructure on the transients detected by fast spectroscopy related to the long-range bacterial inactivation performance. The different fast kinetic femtosecond transient spectroscopy is reported for each FeOx+TiO2 microstructure. The lifetime of the short transient-species and the oxidative intermediate radicals generated under light were identified. Co-sputtered FeOx-TiO2 on polyethylene films presenting random distribution for both oxides were compared with sequentially sputtered FeOx/TiO2 films made up only by FeOx in the topmost layers. The ratio FeOx:TiO2 was optimized to attain the highest photo-conversion. By X-ray fluorescence, the Fe:Ti ration was found to be ~1.4 in the film bulk and by XPS-etching a ratio of 4:1 was found on the photocatalyst top-most layers. For co-sputtered FeOx-TiO2-PE films, the FeOx-TiO2 heterojunction led to electron injection from the FeOx to lower-lying TiO2 trapping states. The film optical properties, particle size, roughness, hydrophobic-hydrophilic shift and temporal evolution of the transient redox states were characterized in detail. Films with different microstructure led to different antibacterial activity. This suggests that the FeOx-TiO2-PE microstructure and not the position of the potential energy level of the semiconductors FeOx and TiO2 control the charge transfer under light irradiation.

  4. FeOx-TiO2 Film with Different Microstructures Leading to Femtosecond Transients with Different Properties: Biological Implications under Visible Light.

    PubMed

    Rtimi, Sami; Pulgarin, Cesar; Nadtochenko, Victor A; Gostev, Fedor E; Shelaev, Ivan V; Kiwi, John

    2016-07-22

    This study presents the first report addressing the effect of FeOx-TiO2 films microstructure on the transients detected by fast spectroscopy related to the long-range bacterial inactivation performance. The different fast kinetic femtosecond transient spectroscopy is reported for each FeOx+TiO2 microstructure. The lifetime of the short transient-species and the oxidative intermediate radicals generated under light were identified. Co-sputtered FeOx-TiO2 on polyethylene films presenting random distribution for both oxides were compared with sequentially sputtered FeOx/TiO2 films made up only by FeOx in the topmost layers. The ratio FeOx:TiO2 was optimized to attain the highest photo-conversion. By X-ray fluorescence, the Fe:Ti ration was found to be ~1.4 in the film bulk and by XPS-etching a ratio of 4:1 was found on the photocatalyst top-most layers. For co-sputtered FeOx-TiO2-PE films, the FeOx-TiO2 heterojunction led to electron injection from the FeOx to lower-lying TiO2 trapping states. The film optical properties, particle size, roughness, hydrophobic-hydrophilic shift and temporal evolution of the transient redox states were characterized in detail. Films with different microstructure led to different antibacterial activity. This suggests that the FeOx-TiO2-PE microstructure and not the position of the potential energy level of the semiconductors FeOx and TiO2 control the charge transfer under light irradiation.

  5. Transferrin-PEG-PE modified dexamethasone conjugated cationic lipid carrier mediated gene delivery system for tumor-targeted transfection

    PubMed Central

    Wang, Wei; Zhou, Fang; Ge, Linfu; Liu, Ximin; Kong, Fansheng

    2012-01-01

    Background The main barriers to non-viral gene delivery include cellular and nuclear membranes. As such, the aim of this study was to develop a type of vector that can target cells through receptor-mediated pathways and by using nuclear localization signal (NLS) to increase the nuclear uptake of genetic materials. Methods A dexamethasone (Dexa)-conjugated lipid was synthesized as the material of the solid lipid nanoparticles (SLNs), and transferrin (Tf) was linked onto polyethylene glycol-phosphatidylethanolamine (PEG-PE) to obtain Tf-PEG-PE ligands for the surface modification of the carriers. The in vitro transfection efficiency of the novel modified vectors was evaluated in human hepatoma carcinoma cell lines, and in vivo effects were observed in an animal model. Results Tf-PEG-PE modified SLNs/enhanced green fluorescence protein plasmid (pEGFP) had a particle size of 222 nm and a gene loading quantity of 90%. Tf-PEG-PE-modified SLNs/pEGFP (Tf-SLNs/pEGFP) displayed remarkably higher transfection efficiency than non-modified SLNs/pEGFP and the vectors not containing Dexa, both in vitro and in vivo. Conclusion It can be concluded that Tf and Dexa could function as an excellent active targeting ligand to improve the cell targeting and nuclear targeting ability of the carriers, and the resulting nanomedicine could be a promising active targeting drug/gene delivery system. PMID:22679364

  6. Quantifying the effects of sterilization and aging on the oxidative degradation and wear of crosslinked and conventional polyethylene used in total joint replacement

    NASA Astrophysics Data System (ADS)

    Willie, Bettina Maria

    2005-07-01

    Nearly 500,000 total knee and hip replacements are performed annually in the United States. The generation of ultra-high molecular weight polyethylene (PE) particulate wear debris and associated osteolysis has increasingly become the predominant cause of revision operation. Research has shown that radiation sterilization in air results in increased oxidative degradation and accelerated wear of PE components. The overall goal of this work was to better understand the effect of sterilization, radiation crosslinking, and aging on the oxidative degradation and wear performance of PE components in order to improve clinical outcomes in total joint replacement. The data indicated that after four years of real-time shelf aging, PE that was radiation sterilized in air or nitrogen had significantly greater oxidative degradation compared to PE that was sterilized with either gas plasma or ethylene oxide. After two years of real-time shelf aging, negligible oxidation occurred with minimal changes in density and percent crystallinity, indicating that oxidative degradation was not an issue in the highly crosslinked and conventional polyethylene components examined. The differences measured between time zero and two years shelf aging may be likely explained by instrumentation error or variation within polyethylene manufacturing lots. Data suggest that current manufacturing and packaging technologies have successfully avoided oxidative degradation during shelf aging. Shelf aging may not be a concern in highly crosslinked or conventional polyethylene with current packaging technologies. Conventional PE tibial components had significantly greater percent area of premelt total surface damage compared to crosslinked PE tibial components. However, conventional PE tibial components did not have a significantly different percent area of postmelt total surface damage compared to crosslinked PE tibial components. Data indicated that in vivo duration was a significant predictor of premelt

  7. New CO2 adsorbent containing aminated poly(glycidyl methacrylate) grafted onto irradiated PE-PP nonwoven sheet

    NASA Astrophysics Data System (ADS)

    Mahmoud Nasef, Mohamed; Abbasi, Ali; Ting, T. M.

    2014-10-01

    A new CO2 adsorbent containing triethylamine (TEA) was prepared by radiation induced grafting of glycidyl methacrylate (GMA) onto polyethylene coated polypropylene (PE-PP) non-woven sheet followed by amination reaction. The degree of grafting (DOG%) was controlled by variation of monomer concentration and absorbed dose. The incorporation of aminated poly(GMA) was investigated by Fourier transform infrared (FTIR) and scanning electron microscope (SEM). The adsorbent with DOG of 350% and amination yield of 60% exhibited CO2 adsorption capacity of 4.52 mol/kg at ambient temperature and pressure.

  8. Transport mechanisms through PE-CVD coatings: influence of temperature, coating properties and defects on permeation of water vapour

    NASA Astrophysics Data System (ADS)

    Kirchheim, Dennis; Jaritz, Montgomery; Mitschker, Felix; Gebhard, Maximilian; Brochhagen, Markus; Hopmann, Christian; Böke, Marc; Devi, Anjana; Awakowicz, Peter; Dahlmann, Rainer

    2017-03-01

    Gas transport mechanisms through plastics are usually described by the temperature-dependent Arrhenius-model and compositions of several plastic layers are represented by the CLT. When it comes to thin films such as plasma-enhanced chemical vapour deposition (PE-CVD) or plasma-enhanced atomic layer deposition (PE-ALD) coatings on substrates of polymeric material, a universal model is lacking. While existing models describe diffusion through defects, these models presume that permeation does not occur by other means of transport mechanisms. This paper correlates the existing transport models with data from water vapour transmission experiments.

  9. Comparative studies of global migration levels of recycled vs virgin polyethylene for packing and storage of milk.

    PubMed

    Upender; Srivastava, M K; Singh, P; Chopra, S

    2003-04-01

    The use of Low-density polyethylene (LDPE) is increased for packaging and storage of food, milk etc. Virgin polyethylene is safe due to non-toxic, inertness and insoluble in milk. It is a replacement of conventional bottle packing of milk. Detection of contamination of milk contact of LDPE film in which milk was packed is being done by global migration method. LDPE films developed by well known technique i.e. Blown film extrusion technique, containing different ratio of virgin-recycled polyethylene materials as well as additives such antioxidants, filler, colourant etc. The impact of above LDPE films on the quality of milk was studied by global migration testing. After analyzing the observed results, it is found that the values of global migration increase with increase in percentage of recycled granules and percentage and type of additives in the film.

  10. Direct and Indirect Polymer-Polymer Interfacial Slip Measurements in Multilayered Films

    NASA Astrophysics Data System (ADS)

    Lee, Patrick C.; Park, Hee Eon; Macosko, Christopher W.

    2008-07-01

    Significant slip can occur during flow of two immiscible polymers due to reduced entanglements at their interface. The slip is of practical importance because of its effect on morphology and adhesion of these multi-phase materials, such as disordered two-phase blends and multilayer films. In this research, we are investigating the amount of polymer-polymer slip over a range of shear stresses from rheological measurements (i.e., indirect method) and visualization measurements (i.e., direct method) on co-extruded multilayer films. Two types of alternately layered blends were chosen: polypropylene (PP)/polystyrene (PS) and polyethylene (PE)/fluoropolymer (FP) blends. The multilayer samples of both PP/PS and PE/FP blends were prepared in a co-extrusion setup (Zhao and Macosko J. Rheol. 2002) at 200 and 210 °C, respectively, in order to match viscosity and linear viscoelasticity. To study the polymer-polymer interfacial slip over a wide stress range, three types of rheometers were used: an in-line slit-die rheometer, a rotational parallel-disk rheometer, and a sliding-plates rheometer (SPR). It was observed that the viscosity of a multilayer sample is lower than the harmonic average viscosity of two neat polymers for both PP/PS and PE/FP and decreases with the number of layers above a certain critical shear stress. Two visualization techniques, (i) the SPR with a glass top plate and (ii) a high temperature shearing cell, were utilized to prove the slip. The slip velocity (i.e., the amount of macroscopic velocity discontinuity at the interface) with respect to shear stress was calculated from each rheological and visualization methods and compared.

  11. From PE Experiences to PE Teaching Practices? Insights from Scottish Primary Teachers' Experiences of PE, Teacher Education, School Entry and Professional Development

    ERIC Educational Resources Information Center

    Elliot, Dely L.; Atencio, Matthew; Campbell, Theresa; Jess, Mike

    2013-01-01

    Morgan and Hansen suggest that further research is needed to explore how non-specialist primary teachers approach and teach physical education (PE) based on their personal school PE backgrounds, teacher education experiences and ongoing professional development. This paper adopts Lawson's socialisation model, a theoretical framework subsequently…

  12. Effect of surface pretreatment of TiO2 films on interfacial processes leading to bacterial inactivation in the dark and under light irradiation.

    PubMed

    Rtimi, Sami; Nesic, Jelena; Pulgarin, Cesar; Sanjines, Rosendo; Bensimon, Michael; Kiwi, John

    2015-02-06

    Evidence is presented for radio-frequency plasma pretreatment enhancing the amount and adhesion of TiO2 sputtered on polyester (PES) and on polyethylene (PE) films. Pretreatment is necessary to attain a suitable TiO2 loading leading to an acceptable Escherichia coli reduction kinetics in the dark or under light irradiation for PES-TiO2 and PE-TiO2 samples. The amount of TiO2 on the films was monitored by diffuse reflectance spectroscopy and X-ray fluorescence. X-ray electron spectroscopy shows the lack of accumulation of bacterial residues such as C, N and S during bacterial inactivation since they seem to be rapidly destroyed by TiO2 photocatalysis. Evidence was found for Ti(4+)/Ti(3+) redox catalysis occurring on PES-TiO2 and PE-TiO2 during the bacterial inactivation process. On PE-TiO2 surfaces, Fourier transform infrared spectroscopy (ATR-FTIR) provides evidence for a systematic shift of the na(CH2) stretching vibrations preceding bacterial inactivation within 60 min. The discontinuous IR-peak shifts reflect the increase in the C-H inter-bond distance leading to bond scission. The mechanism leading to E. coli loss of viability on PES-TiO2 was investigated in the dark up to complete bacterial inactivation by monitoring the damage in the bacterial outer cell by transmission electron microscopy. After 30 min, the critical step during the E. coli inactivation commences for dark disinfection on 0.1-5% wt PES-TiO2 samples. The interactions between the TiO2 aggregates and the outer lipopolysaccharide cell wall involve electrostatic effects competing with the van der Waals forces.

  13. Influence of nuclear interactions in polyethylene range compensators for carbon-ion radiotherapy

    SciTech Connect

    Kanematsu, Nobuyuki Koba, Yusuke; Ogata, Risa; Himukai, Takeshi

    2014-07-15

    Purpose: A recent study revealed that polyethylene (PE) would cause extra carbon-ion attenuation per range shift by 0.45%/cm due to compositional differences in nuclear interactions. The present study aims to assess the influence of PE range compensators on tumor dose in carbon-ion radiotherapy. Methods: Carbon-ion radiation was modeled to be composed of primary carbon ions and secondary particles, for each of which the dose and the relative biological effectiveness (RBE) were estimated at a tumor depth in the middle of spread-out Bragg peak. Assuming exponential behavior for attenuation and yield of these components with depth, the PE effect on dose was calculated for clinical carbon-ion beams and was partly tested by experiment. The two-component model was integrated into a treatment-planning system and the PE effect was estimated in two clinical cases. Results: The attenuation per range shift by PE was 0.1%–0.3%/cm in dose and 0.2%–0.4%/cm in RBE-weighted dose, depending on energy and range-modulation width. This translates into reduction of RBE-weighted dose by up to 3% in extreme cases. In the treatment-planning study, however, the effect on RBE-weighted dose to tumor was typically within 1% reduction. Conclusions: The extra attenuation of primary carbon ions in PE was partly compensated by increased secondary particles for tumor dose. In practical situations, the PE range compensators would normally cause only marginal errors as compared to intrinsic uncertainties in treatment planning, patient setup, beam delivery, and clinical response.

  14. Electrospun Polyaniline/Polyethylene Oxide Nanofiber Field Effect Transistor

    NASA Technical Reports Server (NTRS)

    Pinto, N. J.; Johnson, A. T.; MacDiarmid, A. G.; Mueller, C. H.; Theofylaktos, N.; Robinson, D. C.; Miranda, F. A.

    2003-01-01

    We report on the observation of field effect transistor (FET) behavior in electrospun camphorsulfonic acid doped polyaniline(PANi)/polyethylene oxide(PE0) nanofibers. Saturation channel currents are observed at surprisingly low source/drain voltages. The hole mobility in the depletion regime is 1.4 x 10(exp -4) sq cm/V s while the 1-D charge density (at zero gate bias) is calculated to be approximately 1 hole per 50 two-ring repeat units of polyaniline, consistent with the rather high channel conductivity (approx. 10(exp -3) S/cm). Reducing or eliminating the PEO content in the fiber is expected to enhance device parameters. Electrospinning is thus proposed as a simple method of fabricating 1-D polymer FET's.

  15. Production and characterization of polyethylene/organoclay oriented fiber

    NASA Astrophysics Data System (ADS)

    Coppola, B.; Di Maio, L.; Scarfato, P.; Incarnato, L.

    2016-05-01

    The aim of this work was to study the influence of drawing process on the mechanical properties of polyethylene/clay fibers. To this extent, three different PE/clay blends (3, 5 and 10 wt.%) were prepared by melt compounding in a twin-screw extruder. The investigated clay was a commercial organically modified montmorillonite (Dellite 67G). After compounding fibers were produced by a single-screw extruder and drawn at different draw ratios. At increasing draw ratio an increase of elastic modulus and tensile strength was attained. The presence of clay layers increases fibers ductility hindering fibrils formation during the drawing process. Moreover, at increasing clay contents a decrease of tensile strength for high draw ratios was observed. These results demonstrated that the dispersed clay layers can be re-aggregated by the uniaxial flow induced by the drawing process resulting in a decay of mechanical properties at high draw ratios.

  16. Reinforced polyethylene/clay nanocomposites: influence of different silane

    NASA Astrophysics Data System (ADS)

    Yin, Ming; Zhang, Liying; Chen, Xuelong; Hu, Xiao

    2015-03-01

    Montmorillonite (MMT) was first cation exchanged by cetyltrimethyl ammonium bromide (CTAB) and then treated by short chain silane (methyltrimethoxylsilane) or different amount of long chain silane (dodecyltrimethoxylsilane). High density polyethylene (HDPE)/clay nanocomposites were prepared through twin screw extruder using these silane modified clays without any compatibilizer. Thermal gravimetric analysis (TGA) proved the successful grafting of silanes onto clay. The effects of the chain length and content of the silanes on the dispersion state of clay and properties of the composites were studied using X-ray diffraction (XRD), transmission electron microscope (TEM), mechanical tests, creep tests and so on. The results indicate that the grafting of long chain silanes at higher content could improve the compatibility between clay and PE, thus more efficiently enhancing mechanical and creep properties of the composites than other silane treated clays.

  17. Role of edible film and coating additives

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Edible films and coatings have received increasing interest because films and coatings can carry a diversity of functional ingredients. Plasticizers, such as glycerol, acetylated monoglycerides, polyethylene glycol, and sucrose are often used to modify the mechanical properties of the film or coatin...

  18. Interaction of High Flash Point Electrolytes and PE-Based Separators for Li-Ion Batteries.

    PubMed

    Hofmann, Andreas; Kaufmann, Christoph; Müller, Marcus; Hanemann, Thomas

    2015-08-27

    In this study, promising electrolytes for use in Li-ion batteries are studied in terms of interacting and wetting polyethylene (PE) and particle-coated PE separators. The electrolytes are characterized according to their physicochemical properties, where the flow characteristics and the surface tension are of particular interest for electrolyte-separator interactions. The viscosity of the electrolytes is determined to be in a range of η = 4-400 mPa∙s and surface tension is finely graduated in a range of γL = 23.3-38.1 mN∙m(-1). It is verified that the technique of drop shape analysis can only be used in a limited matter to prove the interaction, uptake and penetration of electrolytes by separators. Cell testing of Li|NMC half cells reveals that those cell results cannot be inevitably deduced from physicochemical electrolyte properties as well as contact angle analysis. On the other hand, techniques are more suitable which detect liquid penetration into the interior of the separator. It is expected that the results can help fundamental researchers as well as users of novel electrolytes in current-day Li-ion battery technologies for developing and using novel material combinations.

  19. Interaction of High Flash Point Electrolytes and PE-Based Separators for Li-Ion Batteries

    PubMed Central

    Hofmann, Andreas; Kaufmann, Christoph; Müller, Marcus; Hanemann, Thomas

    2015-01-01

    In this study, promising electrolytes for use in Li-ion batteries are studied in terms of interacting and wetting polyethylene (PE) and particle-coated PE separators. The electrolytes are characterized according to their physicochemical properties, where the flow characteristics and the surface tension are of particular interest for electrolyte–separator interactions. The viscosity of the electrolytes is determined to be in a range of η = 4–400 mPa∙s and surface tension is finely graduated in a range of γL = 23.3–38.1 mN∙m−1. It is verified that the technique of drop shape analysis can only be used in a limited matter to prove the interaction, uptake and penetration of electrolytes by separators. Cell testing of Li|NMC half cells reveals that those cell results cannot be inevitably deduced from physicochemical electrolyte properties as well as contact angle analysis. On the other hand, techniques are more suitable which detect liquid penetration into the interior of the separator. It is expected that the results can help fundamental researchers as well as users of novel electrolytes in current-day Li-ion battery technologies for developing and using novel material combinations. PMID:26343636

  20. Processing-structure-property studies of: (I) submicron polymeric fibers produced by electrospinning and (II) films of linear low density polyethylenes as influenced by the short chain branch length in copolymers of ethylene/1-butene, ethylene/1-hexene and ethylene/1-octene synthesized by a single site metallocene catalyst

    NASA Astrophysics Data System (ADS)

    Gupta, Pankaj

    The overall theme of the research discussed in this dissertation has been to explore processing-structure-property relationships for submicron polymeric fibers produced by electrospinning (Part I) and to ascertain whether or not the length of the short chain branch has any effect on the physical properties of films of linear low-density polyethylenes (LLDPEs) (Part II). The research efforts discussed in Part I of this dissertation relate to some fundamental as well as more applied investigations involving electrospinning. These include investigating the effects of solution rheology on fiber formation and developing novel methodologies to fabricate polymeric mats comprising of high specific surface submicron fibers of more than one polymer, high chemical resistant substrates produced by in situ photo crosslinking during electrospinning, superparamagnetic flexible substrates by electrospinning a solution of an elastomeric polymer containing ferrite nanoparticles of Mn-Zn-Ni and substrates for filtration applications. Bicomponent electrospinning of poly(vinyl chloride)-polyurethane and poly(vinylidiene fluoride)-polyurethane was successfully performed. In addition, filtration properties of single and bicomponent electrospun mats of polyacrylonitrile and polystyrene were investigated. Results indicated lower aerosol penetration or higher filtration efficiencies of the filters based on submicron electrospun fibers in comparison to the conventional filter materials. In addition, Part II of this dissertation explores whether or not the length of the short chain branch affects the physical properties of blown and compression molded films of LLDPEs that were synthesized by a single site metallocene catalyst. Here, three resins based on copolymers of ethylene/1-butene, ethylene/1-hexene, and ethylene/1-octene were utilized that were very similar in terms of their molecular weight and distribution, melt rheology, density, crystallinity and short chain branching content and

  1. Microwave-assisted fibrous decoration of mPE surface utilizing Aloe vera extract for tissue engineering applications.

    PubMed

    Balaji, Arunpandian; Jaganathan, Saravana Kumar; Supriyanto, Eko; Muhamad, Ida Idayu; Khudzari, Ahmad Zahran Md

    2015-01-01

    Developing multifaceted, biocompatible, artificial implants for tissue engineering is a growing field of research. In recent times, several works have been reported about the utilization of biomolecules in combination with synthetic materials to achieve this process. Accordingly, in this study, the ability of an extract obtained from Aloe vera, a commonly used medicinal plant in influencing the biocompatibility of artificial material, is scrutinized using metallocene polyethylene (mPE). The process of coating dense fibrous Aloe vera extract on the surface of mPE was carried out using microwaves. Then, several physicochemical and blood compatibility characterization experiments were performed to disclose the effects of corresponding surface modification. The Fourier transform infrared spectrum showed characteristic vibrations of several active constituents available in Aloe vera and exhibited peak shifts at far infrared regions due to aloe-based mineral deposition. Meanwhile, the contact angle analysis demonstrated a drastic increase in wettability of coated samples, which confirmed the presence of active components on glazed mPE surface. Moreover, the bio-mimic structure of Aloe vera fibers and the influence of microwaves in enhancing the coating characteristics were also meticulously displayed through scanning electron microscopy micrographs and Hirox 3D images. The existence of nanoscale roughness was interpreted through high-resolution profiles obtained from atomic force microscopy. And the extent of variations in irregularities was delineated by measuring average roughness. Aloe vera-induced enrichment in the hemocompatible properties of mPE was established by carrying out in vitro tests such as activated partial thromboplastin time, prothrombin time, platelet adhesion, and hemolysis assay. In conclusion, the Aloe vera-glazed mPE substrate was inferred to attain desirable properties required for multifaceted biomedical implants.

  2. Microwave-assisted fibrous decoration of mPE surface utilizing Aloe vera extract for tissue engineering applications

    PubMed Central

    Balaji, Arunpandian; Jaganathan, Saravana Kumar; Supriyanto, Eko; Muhamad, Ida Idayu; Khudzari, Ahmad Zahran Md

    2015-01-01

    Developing multifaceted, biocompatible, artificial implants for tissue engineering is a growing field of research. In recent times, several works have been reported about the utilization of biomolecules in combination with synthetic materials to achieve this process. Accordingly, in this study, the ability of an extract obtained from Aloe vera, a commonly used medicinal plant in influencing the biocompatibility of artificial material, is scrutinized using metallocene polyethylene (mPE). The process of coating dense fibrous Aloe vera extract on the surface of mPE was carried out using microwaves. Then, several physicochemical and blood compatibility characterization experiments were performed to disclose the effects of corresponding surface modification. The Fourier transform infrared spectrum showed characteristic vibrations of several active constituents available in Aloe vera and exhibited peak shifts at far infrared regions due to aloe-based mineral deposition. Meanwhile, the contact angle analysis demonstrated a drastic increase in wettability of coated samples, which confirmed the presence of active components on glazed mPE surface. Moreover, the bio-mimic structure of Aloe vera fibers and the influence of microwaves in enhancing the coating characteristics were also meticulously displayed through scanning electron microscopy micrographs and Hirox 3D images. The existence of nanoscale roughness was interpreted through high-resolution profiles obtained from atomic force microscopy. And the extent of variations in irregularities was delineated by measuring average roughness. Aloe vera-induced enrichment in the hemocompatible properties of mPE was established by carrying out in vitro tests such as activated partial thromboplastin time, prothrombin time, platelet adhesion, and hemolysis assay. In conclusion, the Aloe vera-glazed mPE substrate was inferred to attain desirable properties required for multifaceted biomedical implants. PMID:26425089

  3. Hydrogen-hydrogen intermolecular structure of polyethylene in the melt

    NASA Astrophysics Data System (ADS)

    Londono, J. D.; Annis, B. K.; Habenschuss, A.; Smith, G. D.; Borodin, O.; Tso, C.; Hsieh, E. T.; Soper, A. K.

    1999-05-01

    Three polyethylene samples, which differed in their degree of deuteration, were studied in neutron diffraction isotopic substitution (NDIS) experiments at 428 K. These results were complemented at small wavevectors by small angle neutron measurements. The intermolecular hydrogen-hydrogen (HH) structure function, hHH(Q), was obtained without recourse to intramolecular structure models, as demonstrated in a prior report. The PE experimental results are compared to computer simulation results for the alkanes C100 at 509 K and C44 at 350, 400, and 450 K. The small temperature dependence of the HH intermolecular radial distribution functions, gHH(r) for C44 indicates that the differences observed between the PE, C100, and C44 (450 K) results are, for the most part, not due to just temperature differences. It is shown that the string model, an analytic result from an integral equation theory of polymers (PRISM), can account approximately for the overall shape of the gHH(r) functions, and that this overall shape is dependent on the radius of gyration of the molecule. Further analysis shows that there are two other contributions to gHH(r), both of which are independent of chain length to first order. The first is due to chain-chain packing, and the second is due to local HH intermolecular correlations. These results are significant because they demonstrate that hHH(Q) is a useful function for studying intermolecular polymer structure, which has been shown to underpin phase behavior in polyolefin blends.

  4. Chain Ends and the Ultimate Tensile Strength of Polyethylene Fibers

    NASA Astrophysics Data System (ADS)

    O'Connor, Thomas C.; Robbins, Mark O.

    Determining the tensile yield mechanisms of oriented polymer fibers remains a challenging problem in polymer mechanics. By maximizing the alignment and crystallinity of polyethylene (PE) fibers, tensile strengths σ ~ 6 - 7 GPa have been achieved. While impressive, first-principal calculations predict carbon backbone bonds would allow strengths four times higher (σ ~ 20 GPa) before breaking. The reduction in strength is caused by crystal defects like chain ends, which allow fibers to yield by chain slip in addition to bond breaking. We use large scale molecular dynamics (MD) simulations to determine the tensile yield mechanism of orthorhombic PE crystals with finite chains spanning 102 -104 carbons in length. The yield stress σy saturates for long chains at ~ 6 . 3 GPa, agreeing well with experiments. Chains do not break but always yield by slip, after nucleation of 1D dislocations at chain ends. Dislocations are accurately described by a Frenkel-Kontorova model, parametrized by the mechanical properties of an ideal crystal. We compute a dislocation core size ξ = 25 . 24 Å and determine the high and low strain rate limits of σy. Our results suggest characterizing such 1D dislocations is an efficient method for predicting fiber strength. This research was performed within the Center for Materials in Extreme Dynamic Environments (CMEDE) under the Hopkins Extreme Materials Institute at Johns Hopkins University. Financial support was provided by Grant W911NF-12-2-0022.

  5. Biodegradation of polyethylene microplastics by the marine fungus Zalerion maritimum.

    PubMed

    Paço, Ana; Duarte, Kátia; da Costa, João P; Santos, Patrícia S M; Pereira, R; Pereira, M E; Freitas, Ana C; Duarte, Armando C; Rocha-Santos, Teresa A P

    2017-05-15

    Plastic yearly production has surpassed the 300milliontons mark and recycling has all but failed in constituting a viable solution for the disposal of plastic waste. As these materials continue to accumulate in the environment, namely, in rivers and oceans, in the form of macro-, meso-, micro- and nanoplastics, it becomes of the utmost urgency to find new ways to curtail this environmental threat. Multiple efforts have been made to identify and isolate microorganisms capable of utilizing synthetic polymers and recent results point towards the viability of a solution for this problem based on the biodegradation of plastics resorting to selected microbial strains. Herein, the response of the fungus Zalerion maritimum to different times of exposition to polyethylene (PE) pellets, in a minimum growth medium, was evaluated, based on the quantified mass differences in both the fungus and the microplastic pellets used. Additionally, molecular changes were assessed through attenuated total reflectance Fourier transform Infrared Spectroscopy (FTIR-ATR) and Nuclear Magnetic Resonance (NMR). Results showed that, under the tested conditions, Z. maritimum is capable of utilizing PE, resulting in the decrease, in both mass and size, of the pellets. These results indicate that this naturally occurring fungus may actively contribute to the biodegradation of microplastics, requiring minimum nutrients.

  6. Fracture characteristics of balloon films

    NASA Technical Reports Server (NTRS)

    Portanova, Marc A.

    1989-01-01

    An attempt was made to determine the failure modes of high altitude scientific balloons through an investigation of the fracture characteristics of the thin polyethylene films. Two films were the subject of the evaluation, Winzen Int.'s Stratafilm SF-85 and Raven Industries' Astro-E. Research began with an investigation of the film's cold brittleness point and it's effect on the ultimate strength and elasticity of the polyethylene film. A series of preliminary investigations were conducted to develop an understanding of the material characteristics. The primary focus of this investigation was on the notch sensitivity of the films. Simple stress strain tests were also conducted to enable analysis employing fracture toughness parameters. Studies were conducted on both film types at 23 C (room temperature), -60 C, -90 C, and -120 C.

  7. PE11, a PE/PPE family protein of Mycobacterium tuberculosis is involved in cell wall remodeling and virulence

    PubMed Central

    Singh, Parul; Rao, Rameshwaram Nagender; Reddy, Jala Ram Chandra; Prasad, RBN; Kotturu, Sandeep Kumar; Ghosh, Sudip; Mukhopadhyay, Sangita

    2016-01-01

    The role of the unique proline-glutamic acid (PE)/proline-proline-glutamic acid (PPE) family of proteins in the pathophysiology and virulence of Mycobacterium tuberculosis is not clearly understood. One of the PE family proteins, PE11 (LipX or Rv1169c), specific to pathogenic mycobacteria is found to be over-expressed during infection of macrophages and in active TB patients. In this study, we report that M. smegmatis expressing PE11 (Msmeg-PE11) exhibited altered colony morphology and cell wall lipid composition leading to a marked increase in resistance against various environmental stressors and antibiotics. The cell envelope of Msmeg-PE11 also had greater amount of glycolipids and polar lipids. Msmeg-PE11 was found to have better survival rate in infected macrophages. Mice infected with Msmeg-PE11 had higher bacterial load, showed exacerbated organ pathology and mortality. The liver and lung of Msmeg-PE11-infected mice also had higher levels of IL-10, IL-4 and TNF-α cytokines, indicating a potential role of this protein in mycobacterial virulence. PMID:26902658

  8. Extrusion foaming of protein-based thermoplastic and polyethylene blends

    NASA Astrophysics Data System (ADS)

    Gavin, Chanelle; Lay, Mark C.; Verbeek, Casparus J. R.

    2016-03-01

    Currently the extrusion foamability of Novatein® Thermoplastic Protein (NTP) is being investigated at the University of Waikato in collaboration with the Biopolymer Network Ltd (NZ). NTP has been developed from bloodmeal (>86 wt% protein), a co-product of the meat industry, by adding denaturants and plasticisers (tri-ethylene glycol and water) allowing it to be extruded and injection moulded. NTP alone does not readily foam when sodium bicarbonate is used as a chemical blowing agent as its extensional viscosity is too high. The thermoplastic properties of NTP were modified by blending it with different weight fractions of linear low density polyethylene (LLDPE) and polyethylene grafted maleic anhydride (PE-g-MAH) compatibiliser. Extrusion foaming was conducted in two ways, firstly using the existing water content in the material as the blowing agent and secondly by adding sodium bicarbonate. When processed in a twin screw extruder (L/D 25 and 10 mm die) the material readily expanded due to the internal moisture content alone, with a conditioned expansion ratio of up to ± 0.13. Cell structure was non-uniform exhibiting a broad range cell sizes at various stages of formation with some coalescence. The cell size reduced through the addition of sodium bicarbonate, overall more cells were observed and the structure was more uniform, however ruptured cells were also visible on the extrudate skin. Increasing die temperature and introducing water cooling reduced cell size, but the increased die temperature resulted in surface degradation.

  9. 21 CFR 177.1610 - Polyethylene, chlorinated.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyethylene, chlorinated. 177.1610 Section 177... Components of Single and Repeated Use Food Contact Surfaces § 177.1610 Polyethylene, chlorinated. Chlorinated polyethylene identified in this section may be safely used as articles or components of articles that...

  10. 21 CFR 177.1620 - Polyethylene, oxidized.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polyethylene, oxidized. 177.1620 Section 177.1620... Components of Single and Repeated Use Food Contact Surfaces § 177.1620 Polyethylene, oxidized. Oxidized polyethylene identified in paragraph (a) of this section may be safely used as a component of...

  11. 21 CFR 177.1615 - Polyethylene, fluorinated.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyethylene, fluorinated. 177.1615 Section 177... Components of Single and Repeated Use Food Contact Surfaces § 177.1615 Polyethylene, fluorinated. Fluorinated polyethylene, identified in paragraph (a) of this section, may be safely used as food-contact articles...

  12. 21 CFR 177.1620 - Polyethylene, oxidized.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polyethylene, oxidized. 177.1620 Section 177.1620... Components of Single and Repeated Use Food Contact Surfaces § 177.1620 Polyethylene, oxidized. Oxidized polyethylene identified in paragraph (a) of this section may be safely used as a component of...

  13. 21 CFR 573.780 - Polyethylene.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Polyethylene. 573.780 Section 573.780 Food and... Listing § 573.780 Polyethylene. (a) Identity. Polyethylene consists of basic polymers manufactured by the catalytic polymerization of ethylene. (b) Specifications. (1) For the purposes of this section,...

  14. 21 CFR 177.1620 - Polyethylene, oxidized.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyethylene, oxidized. 177.1620 Section 177.1620... Components of Single and Repeated Use Food Contact Surfaces § 177.1620 Polyethylene, oxidized. Oxidized polyethylene identified in paragraph (a) of this section may be safely used as a component of...

  15. 21 CFR 177.1620 - Polyethylene, oxidized.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyethylene, oxidized. 177.1620 Section 177.1620... Components of Single and Repeated Use Food Contact Surfaces § 177.1620 Polyethylene, oxidized. Oxidized polyethylene identified in paragraph (a) of this section may be safely used as a component of...

  16. 21 CFR 177.1615 - Polyethylene, fluorinated.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polyethylene, fluorinated. 177.1615 Section 177... Components of Single and Repeated Use Food Contact Surfaces § 177.1615 Polyethylene, fluorinated. Fluorinated polyethylene, identified in paragraph (a) of this section, may be safely used as food-contact articles...

  17. 21 CFR 177.1615 - Polyethylene, fluorinated.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyethylene, fluorinated. 177.1615 Section 177... Components of Single and Repeated Use Food Contact Surfaces § 177.1615 Polyethylene, fluorinated. Fluorinated polyethylene, identified in paragraph (a) of this section, may be safely used as food-contact articles...

  18. 76 FR 70896 - Polyethylene Glycol; Tolerance Exemption

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-11-16

    ... AGENCY 40 CFR Part 180 Polyethylene Glycol; Tolerance Exemption AGENCY: Environmental Protection Agency... amu), 17,000; also known as polyethylene glycol, when used as an inert ingredient in a pesticide...(oxyethylene, minimum number average molecular weight (in amu), 17,000; also known as polyethylene...

  19. 21 CFR 573.780 - Polyethylene.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Polyethylene. 573.780 Section 573.780 Food and... Listing § 573.780 Polyethylene. (a) Identity. Polyethylene consists of basic polymers manufactured by the catalytic polymerization of ethylene. (b) Specifications. (1) For the purposes of this section,...

  20. 21 CFR 573.780 - Polyethylene.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Polyethylene. 573.780 Section 573.780 Food and... Listing § 573.780 Polyethylene. (a) Identity. Polyethylene consists of basic polymers manufactured by the catalytic polymerization of ethylene. (b) Specifications. (1) For the purposes of this section,...

  1. 21 CFR 177.1610 - Polyethylene, chlorinated.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polyethylene, chlorinated. 177.1610 Section 177... Components of Single and Repeated Use Food Contact Surfaces § 177.1610 Polyethylene, chlorinated. Chlorinated polyethylene identified in this section may be safely used as articles or components of articles that...

  2. 21 CFR 177.1610 - Polyethylene, chlorinated.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polyethylene, chlorinated. 177.1610 Section 177... Components of Single and Repeated Use Food Contact Surfaces § 177.1610 Polyethylene, chlorinated. Chlorinated polyethylene identified in this section may be safely used as articles or components of articles that...

  3. 21 CFR 573.780 - Polyethylene.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Polyethylene. 573.780 Section 573.780 Food and... Listing § 573.780 Polyethylene. (a) Identity. Polyethylene consists of basic polymers manufactured by the catalytic polymerization of ethylene. (b) Specifications. (1) For the purposes of this section,...

  4. 21 CFR 573.780 - Polyethylene.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Polyethylene. 573.780 Section 573.780 Food and... Listing § 573.780 Polyethylene. (a) Identity. Polyethylene consists of basic polymers manufactured by the catalytic polymerization of ethylene. (b) Specifications. (1) For the purposes of this section,...

  5. 21 CFR 177.1610 - Polyethylene, chlorinated.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyethylene, chlorinated. 177.1610 Section 177... Components of Single and Repeated Use Food Contact Surfaces § 177.1610 Polyethylene, chlorinated. Chlorinated polyethylene identified in this section may be safely used as articles or components of articles that...

  6. 21 CFR 177.1615 - Polyethylene, fluorinated.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polyethylene, fluorinated. 177.1615 Section 177... Components of Single and Repeated Use Food Contact Surfaces § 177.1615 Polyethylene, fluorinated. Fluorinated polyethylene, identified in paragraph (a) of this section, may be safely used as food-contact articles...

  7. Close-packed SiO 2/poly(methyl methacrylate) binary nanoparticles-coated polyethylene separators for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Park, Jang-Hoon; Cho, Joo-Hyun; Park, Woong; Ryoo, Dongjo; Yoon, Su-Jin; Kim, Jong Hun; Jeong, Yeon Uk; Lee, Sang-Young

    In an endeavour to improve not only the thermal shrinkage but also the electrochemical performance of separators in lithium-ion batteries, a novel composite separator is developed, i.e., a close-packed SiO 2/poly(methyl methacrylate) (PMMA) binary nanoparticles-coated polyethylene (PE) separator. The introduction of SiO 2 nanoparticles to the coating layer effectively suppresses thermal shrinkage of the composite separator. In contrast to a SiO 2/PMMA coating layer having a film-shaped PMMA binder, the SiO 2/PMMA binary nanoparticle coating layer employs PMMA particles as a binder. As a consequence, a highly porous structure, i.e., well-connected interstitial voids, is formed between the binary SiO 2 and PMMA nanoparticles. The unique porous morphology allows favourable liquid electrolyte wettability and facile ionic conduction, which play a crucial role in improving cell performance such as the discharge capacity and the C-rate capability of the composite separator.

  8. Wear in conventional and highly cross-linked polyethylene cups: a 5-year follow-up study.

    PubMed

    Olyslaegers, Christophe; Defoort, Koen; Simon, Jean-Pierre; Vandenberghe, Luc

    2008-06-01

    Highly cross-linked polyethylene (XLPE) has been introduced in total hip arthroplasty in an effort to reduce polyethylene wear and the associated periprosthetic osteolysis. Our aim was to demonstrate these reduced wear rates in a 2-dimensional head penetration model and to perform a clinical comparison of both groups using the Harris Hip Score (and SF-36 questionnaire). Sixty hips with a Trilogy XLPE liner (Zimmer) were matched and compared to a control group of 20 conventional Trilogy PE liners (Zimmer). No differences in clinical outcome were seen, but a statistically significant reduction in linear wear was observed in the XLPEgroup, after 5 years. It is clear that, because of the reduction and stabilization of free radicals in polyethylene, a reduction in annual wear can be achieved.

  9. Dose effects of cross-linking polyethylene for total knee arthroplasty on wear performance and mechanical properties.

    PubMed

    Asano, Taiyo; Akagi, Masao; Clarke, Ian C; Masuda, Shingo; Ishii, Tsunehiro; Nakamura, Takashi

    2007-11-01

    Wear performance and mechanical properties of cross-linking polyethylene (XLPE) tibial inserts were investigated using a knee simulator, scanning electron microscopy (SEM), and a small punch test (SPT). Ultrahigh molecular weight PE made from GUR1050 resin was irradiated at doses ranging from 0 to 200 kGy and then machined into tibial inserts followed by annealing. The knee simulator was run for up to four million cycles. As the radiation dose increased from 0 to 100 kGy, the wear rate decreased dramatically, yielding 95% wear reduction at 100 kGy. The microwear features observed by SEM supported the dose-dependent wear reduction. The SPT for XLPE after the simulation test showed that, as the radiation dose increased from 0 to 200 kGy, the ultimate displacement decreased dose-dependently, while the ultimate load increased from 0 to 75 kGy and decreased from 75 to 200 kGy. The resulting toughness of the PE increased to its maximum at a dose of 50 kGy and then decreased with higher doses up to 200 kGy. PE cross-linked with radiation doses from 25 to 75 kGy had greater toughness than virgin, nonirradiated PE. However, PE irradiated with 100 kGy or more had lower toughness than virgin PE. These data suggest that a certain amount of irradiation enhances both wear performance and toughness of PE tibial inserts. Although a certain amount of cross-linking would be effective for clinical application of PE tibial inserts, an optimal radiation dose should be much smaller than that used in current XLPE in total hip arthroplasty.

  10. Preparation and release study of Triclosan in polyethylene/Triclosan anti-bacterial blend.

    PubMed

    Kamalipour, Jamshid; Masoomi, Mahmood; Khonakdar, Hossein Ali; Razavi, Seyed Mohammad Reza

    2016-09-01

    In this study, medium density polyethylene (MDPE) incorporated with Triclosan antibacterial substance has been prepared and Triclosan release rate was investigated. The crystallinity level and matrix polarity, as two significant parameters in antibacterial release control, were studied. Triclosan, a well-established widespread antibacterial agent, was incorporated into medium density polyethylene (MDPE) and Maleic anhydride grafted polyethylene (PE-g-MA) was used to change the polarity of the MDPE matrix. A masterbatch of 10wt% Triclosan incorporated with the MDPE and various PE-g-MA concentrations were prepared using an internal mixer. Then the masterbatch was diluted in the MDPE matrix to produce compounds with 0.1, 0.5, and1wt% Triclosan via twin screw extruder. The compounds were molded by compression molding method and then were cooled in three different cooling rate methods: isothermal cooling (I), quenching (Q),and moderate 5-10°C/min cooling rate (M). Cooling rate effects on crystallinity level were investigated applying sample density measurement. UV-vis absorption spectroscopy was used to probe the release of Triclosan. Antibacterial properties of the compounds against Escherichia coli, Klebsiella pneumoniae, and Staphylococcus aureus were measured. The results showed that by addition of PE-g-MA, Triclosan release rate was increased. It was confirmed that the sample crystallinity was decreased by the cooling rate enhancement. The results also showed that quenched samples indicated higher release of Triclosan. Cooling rate reduction and raising the polarity increased the release of Triclosan and improved the antibacterial properties of the compounds.

  11. An innovative recycling process to obtain pure polyethylene and polypropylene from household waste.

    PubMed

    Serranti, Silvia; Luciani, Valentina; Bonifazi, Giuseppe; Hu, Bin; Rem, Peter C

    2015-01-01

    An innovative recycling process, based on magnetic density separation (MDS) and hyperspectral imaging (HSI), to obtain high quality polypropylene and polyethylene as secondary raw materials, is presented. More in details, MDS was applied to two different polyolefin mixtures coming from household waste. The quality of the two separated PP and PE streams, in terms of purity, was evaluated by a classification procedure based on HSI working in the near infrared range (1000-1700 nm). The classification model was built using known PE and PP samples as training set. The results obtained by HSI were compared with those obtained by classical density analysis carried in laboratory on the same polymers. The results obtained by MDS and the quality assessment of the plastic products by HSI showed that the combined action of these two technologies is a valid solution that can be implemented at industrial level.

  12. Influence of polyethylene microplastic beads on the uptake and localization of silver in zebrafish (Danio rerio).

    PubMed

    Khan, Farhan R; Syberg, Kristian; Shashoua, Yvonne; Bury, Nicolas R

    2015-11-01

    This study aimed to determine whether the uptake and localization of Ag in zebrafish was affected by the presence of polyethylene microplastic beads (PE MPBs). Zebrafish were exposed to 1 μg Ag L(-1) (radiolabelled with (110m)Ag) for 4 and 24 h in the presence or absence of PE MPBs (10, 100 or 1000 MPBs mL(-1)), and one treatment in which MPBs (1000 MPBs mL(-1)) were incubated with Ag to promote adsorption. The presence of MPBs, at any of the tested doses, had no effect on the uptake or localization of Ag. However, exposure to the Ag-incubated MPBs (∽75% of the Ag bound to MPBs) significantly reduced Ag uptake at both time points and also significantly increased the proportion of intestinal Ag. This study demonstrates that microplastics can alter the bioavailability and uptake route of a metal contaminant in a model fish species.

  13. Biodegradation of the composites based on polyethylene and sevilene with natural rubber

    NASA Astrophysics Data System (ADS)

    Kolesnikova, N. N.; Lukanina, Yu. K.; Popov, A. A.

    2013-10-01

    The mechanical properties, the water absorption, and the resistance to soil microrbiota of the composite films based on polyethylene and ethylene-vinyl acetate copolymers with additives of natural rubber are studied. The intensity of the biodegradation of the composites is shown to depend on both the mixture composition and the content of vinyl acetate units in a copolymer.

  14. Evaluation of the impact of polyethylene microbeads ingestion in European sea bass (Dicentrarchus labrax) larvae.

    PubMed

    Mazurais, D; Ernande, B; Quazuguel, P; Severe, A; Huelvan, C; Madec, L; Mouchel, O; Soudant, P; Robbens, J; Huvet, A; Zambonino-Infante, J

    2015-12-01

    Microplastics are present in marine habitats worldwide and may be ingested by low trophic organisms such as fish larvae, with uncertain physiological consequences. The present study aims at assessing the impact of polyethylene (PE 10-45 μM) microbeads ingestion in European sea bass (Dicentrarchus labrax) larvae. Fish were fed an inert diet including 0, 10(4) and 10(5) fluorescent microbeads per gram from 7 until 43 days post-hatching (dph). Microbeads were detected in the gastrointestinal tract in all fish fed diet incorporating PE. Our data revealed an efficient elimination of PE beads from the gut since no fluorescent was observed in the larvae after 48 h depuration. While the mortality rate increased significantly with the amount of microbeads scored per larvae at 14 and 20 dph, only ingestion of the highest concentration slightly impacted mortality rates. Larval growth and inflammatory response through Interleukine-1-beta (IL-1β) gene expression were not found to be affected while cytochrome-P450-1A1 (cyp1a1) expression level was significantly positively correlated with the number of microbeads scored per larva at 20 dph. Overall, these results suggest that ingestion of PE microbeads had limited impact on sea bass larvae possibly due to their high potential of egestion.

  15. Molecular dynamics simulation on adsorption of pyrene-polyethylene onto ultrathin single-walled carbon nanotube

    NASA Astrophysics Data System (ADS)

    Cai, Lu; Lv, Wenzhen; Zhu, Hong; Xu, Qun

    2016-07-01

    The mechanism of the adsorption of pyrene-polyethylene (Py-PE) onto ultrathin single-walled carbon nanotube (SWNT) was studied by using all-atom molecular dynamics (MD) simulations. We found that solvent polarity and pyrene group are two critical factors in the Py-PE decoration on ultrathin SWNT. Combined MD simulations with free energy calculations, our results indicate that larger solvent polarity can decrease the contribution of conformation entropy, but contributes little to the interaction energy, moreover, larger SWNT diameter can decrease the contribution of conformation entropy but lead to the increasing of the interaction energy. In polar organic solvent (N, N-Dimethylacetamide), the pyrene group plays a key role in the adsorption of Py-PE onto ultrathin SWNT, not only facilitates the spontaneous adsorption of Py-PE onto ultrathin SWNT, but also helps to form compact structure between themselves in the final adsorption states. While in aqueous solution, pyrene group no longer works as an anchor, but still affects a lot to the final adsorption conformation. Our present work provides detailed theoretical clue to understand the noncovalent interaction between aromatic segment appended polymer and ultrathin SWNT, and helps to explore the potential application of ultrathin SWNT in the fields of hybrid material, biomedical and electronic materials.

  16. Enhanced blood compatibility of metallocene polyethylene subjected to hydrochloric acid treatment for cardiovascular implants.

    PubMed

    Jaganathan, Saravana Kumar; Mohandas, Hemanth; Sivakumar, Gunalan; Kasi, Palaniappan; Sudheer, Theertha; Avineri Veetil, Sruthi; Murugesan, Selvakumar; Supriyanto, Eko

    2014-01-01

    Blood compatibility of metallocene polyethylene (mPE) was investigated after modifying the surface using hydrochloric acid. Contact angle of the mPE exposed to HCl poses a decrease in its value which indicates increasing wettability and better blood compatibility. Surface of mPE analyzed by using FTIR revealed no significant changes in its functional groups after treatment. Furthermore, scanning electron microscope images supported the increasing wettability through the modifications like pit formations and etching on the acid rendered surface. To evaluate the effect of acid treatment on the coagulation cascade, prothrombin time (PT) and activated partial thromboplastin time (APTT) were measured. Both PT and APTT were delayed significantly (P < 0.05) after 60 min exposure implying improved blood compatibility of the surfaces. Hemolysis assay of the treated surface showed a remarkable decrease in the percentage of lysis of red blood cells when compared with untreated surface. Moreover, platelet adhesion assay demonstrated that HCl exposed surfaces deter the attachment of platelets and thereby reduce the chances of activation of blood coagulation cascade. These results confirmed the enhanced blood compatibility of mPE after HCl exposure which can be utilized for cardiovascular implants like artificial vascular prostheses, implants, and various blood contacting devices.

  17. Interplay between surface properties of standard, vitamin E blended and oxidised ultra high molecular weight polyethylene used in total joint replacement and adhesion of Staphylococcus aureus and Escherichia coli.

    PubMed

    Banche, G; Allizond, V; Bracco, P; Bistolfi, A; Boffano, M; Cimino, A; Brach del Prever, E M; Cuffini, A M

    2014-04-01

    We have assessed the different adhesive properties of some of the most common bacteria associated with periprosthetic joint infection on various types of ultra high molecular Weight Polyethylene (UHMWPE). Quantitative in vitro analysis of the adhesion of biofilm producing strains of Staphylococcus aureus and Escherichia coli to physically and chemically characterised standard UHMWPE (PE), vitamin E blended UHMWPE (VE-PE) and oxidised UHMWPE (OX-PE) was performed using a sonication protocol. A significant decreased bacterial adhesion was registered for both strains on VE-PE, in comparison with that observed on PE, within 48 hours of observation (S. aureus p = 0.024 and E. coli p = 0.008). Since Vitamin E reduces bacterial adhesive ability, VE-stabilised UHMWPE could be valuable in joint replacement by presenting excellent mechanical properties, while reducing bacterial adhesiveness.

  18. Plasma-modified and polyethylene glycol-grafted polymers for potential tissue engineering applications.

    PubMed

    Svorcík, V; Makajová, Z; Kasálková-Slepicková, N; Kolská, Z; Bacáková, L

    2012-08-01

    Modified and grafted polymers may serve as building blocks for creating artificial bioinspired nanostructured surfaces for tissue engineering. Polyethylene (PE) and polystyrene (PS) were modified by Ar plasma and the surface of the plasma activated polymers was grafted with polyethylene glycol (PEG). The changes in the surface wettability (contact angle) of the modified polymers were examined by goniometry. Atomic Force Microscopy (AFM) was used to determine the surface roughness and morphology and electrokinetical analysis (Zeta potential) characterized surface chemistry of the modified polymers. Plasma treatment and subsequent PEG grafting lead to dramatic changes in the polymer surface morphology, roughness and wettability. The plasma treated and PEG grafted polymers were seeded with rat vascular smooth muscle cells (VSMCs) and their adhesion and proliferation were studied. Biological tests, performed in vitro, show increased adhesion and proliferation of cells on modified polymers. Grafting with PEG increases cell proliferation, especially on PS. The cell proliferation was shown to be an increasing function of PEG molecular weight.

  19. Synthesis of Cu{sub 2}ZnSnS{sub 4} nanoparticles and controlling the morphology with polyethylene glycol

    SciTech Connect

    Rawat, Kusum; Kim, Hee-Joon; Shishodia, P.K.

    2016-05-15

    Highlights: • Cu{sub 2}ZnSnS{sub 4} nanoparticles were synthesized by wet chemical technique. • First report on the effect of using polyethylene glycol as a structure directing agent on Cu{sub 2}ZnSnS{sub 4} nanoparticles. • The morphology of Cu{sub 2}ZnSnS{sub 4} nanoparticles changes into nanoflakes and nanorods structures with polyethylene glycol concentration. • Polyethylene glycol assisted Cu{sub 2}ZnSnS{sub 4} nanoparticle film exhibits optical bandgap of 1.5 eV which is suitable for the application in solar cells. - Abstract: Cu{sub 2}ZnSnS{sub 4} nanoparticles were synthesized by wet chemical technique using metal thiourea precursor at 250 °C. The structural and morphological properties of as grown nanoparticles have been characterized by X-ray diffraction, Raman spectroscopy, scanning electron microscopy and transmission electron microscopy. The influence of different concentration of polyethylene glycol as structure directing agent on the morphologies of Cu{sub 2}ZnSnS{sub 4} nanoparticles are investigated on thin films deposited by spin coating technique. The mean crystallite size of the Cu{sub 2}ZnSnS{sub 4} nanoparticles was found to improve with polyethylene glycol concentration. Scanning electron microscopy images of Cu{sub 2}ZnSnS{sub 4} revealed aggregated spherical shaped nanoparticles whereas the polyethylene glycol assisted Cu{sub 2}ZnSnS{sub 4} nanoparticle films show nanoflakes and nanorods structures with increasing concentration of polyethylene glycol. Transmission electron microscopy analysis has also been performed to determine the size and structure of nanorods. UV–vis absorption spectroscopy shows the broad band absorption with optical bandgap of 1.50 eV for polyethylene glycol assisted Cu{sub 2}ZnSnS{sub 4} films.

  20. Effects of Surface Modification and Bulk Geometry on the Biotribological Behavior of Cross-Linked Polyethylene: Wear Testing and Finite Element Analysis

    PubMed Central

    Watanabe, Kenichi; Kyomoto, Masayuki; Saiga, Kenichi; Taketomi, Shuji; Inui, Hiroshi; Kadono, Yuho; Takatori, Yoshio; Tanaka, Sakae; Ishihara, Kazuhiko; Moro, Toru

    2015-01-01

    The wear and creep deformation resistances of polymeric orthopedic bearing materials are both important for extending their longevity. In this study, we evaluated the wear and creep deformation resistances, including backside damage, of different polyethylene (PE) materials, namely, conventional PE, cross-linked PE (CLPE), and poly(2-methacryloyloxyethyl phosphorylcholine)- (PMPC-) grafted CLPE, through wear tests and finite element analysis. The gravimetric and volumetric degrees of wear of disks (3 or 6 mm in thickness) of these materials against a cobalt-chromium-molybdenum alloy pin were examined using a multidirectional pin-on-disk tester. Cross-linking and PMPC grafting decreased the gravimetric wear of the PE disks significantly. The volumetric wear at the bearing surface and the volumetric penetration in the backside of the 3-mm thick PE disk were higher than those of the 6-mm thick PE disk, regardless of the bearing material. The geometrical changes induced in the PE disks consisted of creep, because the calculated internal von Mises stress at the bearing side of all disks and that at the backside of the 3-mm thick disks exceeded their actual yield strengths. A highly hydrated bearing surface layer, formed by PMPC grafting, and a cross-linking-strengthened substrate of adequate thickness are essential for increasing the wear and creep deformation resistances. PMID:26583106